All Stories

  1. Upcycling Hydrofluorocarbons to Valuable Bis(perfluoroalkyl)carbinols via Nucleophilic Fluoroalkylation
  2. Toward a circular fluoropolymer economy coupling PFAS degradation and fluorine reutilization
  3. 2.1 Electrophilic Fluorinating Agents
  4. High-valent sulfur fluorides as reactivity switches for PFAS-free benzene–azepine skeletal editing
  5. From fluorine chemistry to noncovalent interactions: celebrating Prof. Giuseppe Resnati
  6. Bidirectional skeletal remodelling of SF 5 -nitrobenzenes into azepine, bicyclic, and benzimidazole frameworks
  7. Upcycling of PTFE and PVDF to fluorochemicals through mechanochemical process
  8. N -Difluoroacetylation of Sulfoximines by TFEDMA
  9. Cu-Catalyzed SF 4 -Alkynylation of Quinolones, Chromones and Cyclohexenones
  10. From Refrigerant to Reagent: Repurposing HFC-125 into Inorganic and Organic Fluorinating Agents
  11. Recent Advances on Catalytic Asymmetric Synthesis of Molecules Bearing a Fluorine-Containing Stereogenic Carbon Center (2015–2024)
  12. Room-temperature defluorination of PTFE and PFAS via sodium dispersion
  13. Mechanochemical pathway for converting fluoropolymers to fluorochemicals
  14. Synthesis of Silylmethyl gem-Difluoroalkenes via Room-Temperature Catalytic Defluorosilylation of Trifluoromethylalkenes
  15. Breaking the Strongest Organic Bonds by Water: Defluorosubstitutions at the Air–Water Interface of Microdroplets
  16. Repurposing HFC-125 to tetrafluoroethylene: A step toward a more sustainable fluoropolymer feedstock strategy
  17. Nitrogen-Based Organofluorine Functional Molecules: Synthesis and Applications
  18. How Temperature Change Affects the Lattice Parameters, Molecular Conformation, and Reaction Cavity in Enantiomeric and Racemic Crystals of Thalidomide
  19. Discovering Key Activation Hotspots in the M2 Muscarinic Receptor
  20. Radical trifluoromethoxylation of fluorinated alkenes for accessing difluoro(trifluoromethoxy)methyl groups
  21. Chemoselective Cu-catalyzed acylsilylation of vinyl arenes using silylboronates and acyl fluorides
  22. Sequential Michael addition, cross-coupling and [3 + 2] cycloaddition reactions within the coordination sphere of chiral Ni(ii) Schiff base complexes derived from dehydroamino acids: pathways to the asymmetric synthesis of structurally diver...
  23. Synthesis of Ngai Reagent and Longer Carbon Chain Variants for Perfluoroalkoxylations
  24. Stereodivergent Hydrohalogenation of SCF3 Alkynes and Cross- Coupling Reactions
  25. TBHP Promotes Cross-Dehydrogenative Coupling of SF4 Alkynes with Tetrahydroisoquinolines under Copper Catalysis
  26. Mechanochemical Deoxyfluorination of Carboxylic Acids to Acyl Fluorides and Successive Mechanochemical Amide Bond Formation
  27. Cross Dehydrogenative Coupling of SF4-Alkyne with Tetrahydroisoquinolines
  28. Transition‐Metal‐Free Approach for Z‐Vinyl Fluorides by Hydrofluorination of Alkynes bearing SF4 and SF5 Groups
  29. Transition‐Metal‐Free Approach for Z‐Vinyl Fluorides by Hydrofluorination of Alkynes bearing SF4 and SF5 Groups
  30. A silylboronate-mediated strategy for cross-coupling of alkyl fluorides with aryl alkanes: mechanistic insights and scope expansion
  31. Cross-coupling of organic fluorides with allenes: a silyl-radical-relay pathway for the construction of α-alkynyl-substituted all-carbon quaternary centres
  32. Halo-perfluoroalkoxylation of gem-difluoroalkenes with short-lived alkali metal perfluoroalkoxides in triglyme
  33. Expanding the Frontier of Linear Drug Design: Cu‐Catalyzed Csp–Csp3‐Coupling of Electron‐Deficient SF4‐Alkynes with Alkyl Iodides
  34. Preface to the Special Issue on Fluorine Chemistry
  35. Regio‐ and Z‐Selective Alkyne Hydroamination and Hydrophenoxylation using Tetrafluoro‐λ6‐Sulfanyl Alkynes under Superbasic, Naked Anion Conditions
  36. Regio‐ and Z‐Selective Alkyne Hydroamination and Hydrophenoxylation using Tetrafluoro‐λ6‐Sulfanyl Alkynes under Superbasic, Naked Anion Conditions
  37. Current State of Microflow Trifluoromethylation Reactions
  38. Fluorinated Vilsmeier Reagent: TFEDMA‐mediated Synthesis of Aryl‐cyanides and Aryl‐amides via the Activation of Oximes†
  39. N‐Fluoro Ammonium Salts of Cinchona Alkaloids in Enantioselective Electrophilic Fluorination
  40. Elemental Sulfur-Mediated Transformation of Carboxylic Acids to Acyl Fluorides by Electrophilic Fluorinating Reagent, Selectfluor
  41. Transition-metal-free silylboronate-mediated cross-couplings of organic fluorides with amines
  42. Synthesis, Characterization, and Study of Catalytic Activity of Chiral Cu(II) and Ni(II) Salen Complexes in the α-Amino Acid C-α Alkylation Reaction
  43. Synthesis of triarylmethanes by silyl radical-mediated cross-coupling of aryl fluorides and arylmethanes
  44. Lenalidomide Derivative and PROTAC for Controlling Neosubstrate Degradation
  45. KHMDS/Triglyme Cryptate as an Alternative to Phosphazene Base in Stereodivergent Pentafluoroethylation of N-Sulfinylimines Using HFC-125
  46. Unusual Photoisomerization Pathway in a Near-Infrared Light Absorbing Enzymerhodopsin
  47. Etherification of Fluoroarenes with Alkoxyboronic Acid Pinacol Esters via C–F Bond Cleavage
  48. Synthesis of Pyridine–SF4–Isoxazolines Using the Functionality of trans-Tetrafluoro-λ6-sulfanyl Rodlike Linkers
  49. Regioselective Synthesis of Pyridine-SF4-Methyl Ketones via Hydration of Pyridine-SF4-Alkynes
  50. Ethynyl-SF4-Pyridines: Reagents for SF4-Alkynylation to Carbonyl Compounds
  51. Enantio‐, Diastereo‐ and Regioselective Synthesis of Chiral Cyclic and Acyclic gem‐Difluoromethylenes by Palladium‐Catalyzed [4+2] Cycloaddition
  52. Enantio‐, Diastereo‐ and Regioselective Synthesis of Chiral Cyclic and Acyclic gem‐Difluoromethylenes by Palladium‐Catalyzed [4+2] Cycloaddition
  53. Synthesis of an Eccentric Electron-Deficient Fluorinated Motif, Tetrafluoro-λ6-sulfanyl gem-Difluorocyclopropenes
  54. A proximity biotinylation-based approach to identify protein-E3 ligase interactions induced by PROTACs and molecular glues
  55. Construction of poly-N-heterocyclic scaffolds via the controlled reactivity of Cu-allenylidene intermediates
  56. Catalyst-free carbosilylation of alkenes using silyl boronates and organic fluorides via selective C-F bond activation
  57. Diastereodivergent Synthesis of Chiral 4-Fluoropyrrolidines (exo and exo′) Based on the Cu(II)-Catalyzed Asymmetric 1,3-Dipolar Cycloaddition
  58. Pentafluoroethylation of Carbonyl Compounds Using HFC-125 in a Flow Microreactor System
  59. Synthesis of Tetra‐Substituted Trifluoromethyl‐3,1‐Benzoxazines by Transition‐Metal‐Catalyzed Decarboxylative Cyclization of N‐Benzoyl Benzoxazinones
  60. Pentafluoroethylation of Carbonyl Compounds by HFC-125 via the Encapsulation of the K Cation with Glymes
  61. Synthesis of Difluoromethanesulfinate Esters by the Difluoromethanesulfinylation of Alcohols
  62. Synthesis of trifluoromethyl ketones by nucleophilic trifluoromethylation of esters under a fluoroform/KHMDS/triglyme system
  63. Thalidomide and its metabolite 5‐hydroxythalidomide induce teratogenicity via the cereblon neosubstrate PLZF
  64. Acyl Fluorides from Carboxylic Acids, Aldehydes, or Alcohols under Oxidative Fluorination
  65. Transition‐Metal Free Catalytic Synthesis of Trifluoromethyl Indolines by [4+1] Cycloaddition of Trifluoromethyl Benzoxazinones with Sulfur Ylides
  66. Vibrational analysis of acetylcholine binding to the M2 receptor
  67. Deoxyfluorination of acyl fluorides to trifluoromethyl compounds by FLUOLEAD®/Olah’s reagent under solvent-free conditions
  68. Modular Synthesis of Medium-Sized Fluorinated and Nonfluorinated Heterocyclic Lactones by Sequential CN-Bond-Cleaving Ring Expansion under Pd Catalysis
  69. Synthesis of Chiral gem-Difluoromethylene Compounds by Enantioselective Ethoxycarbonyldifluoromethylation of MBH Fluorides via Silicon-Assisted C–F Bond Activation
  70. Design and Synthesis of a Chiral Halogen-Bond Donor with a Sp3-Hybridized Carbon–Iodine Moiety in a Chiral Fluorobissulfonyl Scaffold
  71. An IMiD-induced SALL4 degron system for selective degradation of target proteins
  72. Structural bases of IMiD selectivity that emerges by 5-hydroxythalidomide
  73. Current Contributions of Organofluorine Compounds to the Agrochemical Industry
  74. Diastereoselective Synthesis of Enantioenriched Trifluoromethylated Ethylenediamines and Isoindolines Containing Two Stereogenic Carbon Centers by Nucleophilic Trifluoromethylation Using HFC-23
  75. Pd-catalyzed fluoro-carbonylation of aryl, vinyl, and heteroaryl iodides using 2-(difluoromethoxy)-5-nitropyridine
  76. Contribution of Organofluorine Compounds to Pharmaceuticals
  77. Two Catalytic Annulation Modes via Cu-Allenylidenes with Sulfur Ylides that Are Dominated by the Presence or Absence of Trifluoromethyl Substituents
  78. Synthesis of Both Enantiomers of Nine‐Membered CF3‐Substituted Heterocycles Using a Single Chiral Ligand: Palladium‐Catalyzed Decarboxylative Ring Expansion with Kinetic Resolution
  79. Synthesis of Both Enantiomers of Nine‐Membered CF3‐Substituted Heterocycles Using a Single Chiral Ligand: Palladium‐Catalyzed Decarboxylative Ring Expansion with Kinetic Resolution
  80. Synthesis of Highly Functionalized 12-Membered Trifluoromethyl Heterocycles via a Nondecarboxylative Pd-Catalyzed [6 + 6] Annulation
  81. Pyridine tetrafluoro-λ6-sulfanyl chlorides: spontaneous addition to alkynes and alkenes in the presence or absence of photo-irradiation
  82. Selective synthesis of spirobiindanes, alkenyl chlorides, and monofluoroalkenes from unactivated gem-difluoroalkanes controlled by aluminum-based Lewis acids
  83. Studies of Halogen Bonding Induced by Pentafluorosulfanyl Aryl Iodides: A Potential Group of Halogen Bond Donors in a Rational Drug Design
  84. Studies of Halogen Bonding Induced by Pentafluorosulfanyl Aryl Iodides: A Potential Group of Halogen Bond Donors in a Rational Drug Design
  85. Enantioselective Benzylation and Allylation of α-Trifluoromethoxy Indanones under Phase-Transfer Catalysis
  86. Enantioselective Benzylation and Allylation of α-Trifluoromethoxy Indanones under Phase-Transfer Catalysis
  87. Activation of Saturated Fluorocarbons to Synthesize Spirobiindanes, Monofluoroalkenes, and Indane Derivatives
  88. Cover Feature: Catalytic Desymmetrization of 1,3‐Difluoropropan‐2‐ols via C−F Bond Activation Using a Phosphazene Base Affords Monofluoromethyl‐Substituted Epoxides (Asian J. Org. Chem. 5/2019)
  89. The story of SF5-substituted pyridines
  90. Catalytic Desymmetrization of 1,3‐Difluoropropan‐2‐ols via C−F Bond Activation Using a Phosphazene Base Affords Monofluoromethyl‐Substituted Epoxides
  91. Front Cover: Gas/Liquid‐Phase Micro‐Flow Trifluoromethylation using Fluoroform: Trifluoromethylation of Aldehydes, Ketones, Chalcones, and N‐Sulfinylimines (ChemistryOpen 4/2019)
  92. Pd-Catalyzed Decarboxylative Cyclization of Trifluoromethyl Vinyl Benzoxazinanones with Sulfur Ylides: Access to Trifluoromethyl Dihydroquinolines
  93. Gas/Liquid‐Phase Micro‐Flow Trifluoromethylation using Fluoroform: Trifluoromethylation of Aldehydes, Ketones, Chalcones, and N‐Sulfinylimines
  94. Asymmetric Electrophilic Difluoromethylthiolation of Indanone-Based β-Keto Esters Using Difluoromethanesulfonyl Hypervalent Iodonium Ylides
  95. Synthesis of aryl and heteroaryl tetrafluoro-λ6-sulfanyl chlorides from diaryl disulfides using trichloroisocyanuric acid and potassium fluoride
  96. Understanding the Thalidomide Chirality in Biological Processes by the Self-disproportionation of Enantiomers
  97. Synthesis of Chiral Nonracemic α-Difluoromethylthio Compounds with Tetrasubstituted Stereogenic Centers via a Palladium-Catalyzed Decarboxylative Asymmetric Allylic Alkylation
  98. Defluorosilylation of fluoroarenes and fluoroalkanes
  99. Super-Sensitive Protonation Behavior of Trifluoroethoxy-Substituted Phthalocyanines and Their Application to Solvent Discrimination
  100. Direct nucleophilic trifluoromethylation of carbonyl compounds by potent greenhouse gas, fluoroform: Improving the reactivity of anionoid trifluoromethyl species in glymes
  101. A small-molecule inhibitor of SOD1-Derlin-1 interaction ameliorates pathology in an ALS mouse model
  102. Fluorobissulfonylmethyl Iodides: An Efficient Scaffold for Halogen Bonding Catalysts with an sp3-Hybridized Carbon–Iodine Moiety
  103. Modern Approaches for Asymmetric Construction of Carbon–Fluorine Quaternary Stereogenic Centers: Synthetic Challenges and Pharmaceutical Needs
  104. Highly Diastereoselective Synthesis of Trifluoromethyl Indolines by Interceptive Benzylic Decarboxylative Cycloaddition of Nonvinyl, Trifluoromethyl Benzoxazinanones with Sulfur Ylides under Palladium Catalysis
  105. Synthesis of fluoro-functionalized diaryl-λ3-iodonium salts and their cytotoxicity against human lymphoma U937 cells
  106. Synthesis of Aryl Triflones through the Trifluoromethanesulfonylation of Benzynes
  107. Structural basis of thalidomide enantiomer binding to cereblon
  108. Nucleophilic fluoroalkylation/cyclization route to fluorinated phthalides
  109. Front Cover: Trifluoroethoxy‐Coated Subphthalocyanines Attract Small Arenes in Their π‐Concave Cavity (ChemPlusChem 3/2018)
  110. Trifluoroethoxy‐Coated Subphthalocyanines Attract Small Arenes in Their π‐Concave Cavity
  111. Anionic Triflyldiazomethane: Generation and Its Application for Synthesis of Pyrazole-3-triflones via [3 + 2] Cycloaddition Reaction
  112. Access to benzo-fused nine-membered heterocyclic alkenes with a trifluoromethyl carbinol moiety via a double decarboxylative formal ring-expansion process under palladium catalysis
  113. An eccentric rod-like linear connection of two heterocycles: synthesis of pyridine trans-tetrafluoro-λ6-sulfanyl triazoles
  114. Asymmetric synthesis of α-trifluoromethoxy ketones with a tetrasubstituted α-stereogenic centre via the palladium-catalyzed decarboxylative allylic alkylation of allyl enol carbonates
  115. Design and synthesis of galactose-conjugated fluorinated and non-fluorinated proline oligomers: towards antifreeze molecules
  116. Highly C-selective difluoromethylation of β-ketoesters by using TMSCF2Br/lithium hydroxide/N,N,N-trimethylhexadecan-1-ammonium bromide
  117. Stereodivergent trifluoromethylation of N-sulfinylimines by fluoroform with either organic-superbase or organometallic-base
  118. Stille cross-coupling of secondary and tertiary α-(trifluoromethyl)-benzyl chlorides with allylstannanes
  119. Synthesis of pyridine trans-tetrafluoro-λ6-sulfane derivatives via radical addition
  120. The CF3-DAST-induced deacylative trifluoromethylthiolation of cyclic 1,3-diketones/lactams/lactones and its extension to deacylative pentafluorophenylthiolation
  121. Trifluoroethoxy‐Coated Subphthalocyanines Attract Small Arenes in Their π‐Concave Cavity
  122. Recent advancements in the synthesis of pentafluorosulfanyl (SF5)-containing heteroaromatic compounds
  123. Intramolecular Aminotrifluoromethanesulfinyloxylation of ω-Aminoalkenes by CF3SO2Na/Pd(OAc)2/PhI(OAc)2/ t BuOCl/PivOH System
  124. Synthesis of Sulfur Perfluorophenyl Compounds Using a Pentafluorobenzenesulfonyl Hypervalent Iodonium Ylide
  125. Electrophilic Triflyl-arylation and Triflyl-pyridylation by Unsymmetrical Aryl/Pyridyl-λ3-iodonium Salts: Synthesis of Aryl and Pyridyl Triflones
  126. The Dihydroxy Metabolite of the Teratogen Thalidomide Causes Oxidative DNA Damage
  127. Biological evaluation of both enantiomers of fluoro-thalidomide using human myeloma cell line H929 and others
  128. Trifluoroethoxy-Coated Phthalocyanine Catalyzes Perfluoroalkylation of Alkenes under Visible-Light Irradiation
  129. New utility of electrophilic trifluoromethylthiolation reagents for the synthesis of a variety of triflones
  130. Operationally Convenient and Scalable Asymmetric Synthesis of (2S)‐ and (2R)‐α‐(Methyl)cysteine Derivatives through Alkylation of Chiral Alanine Schiff Base NiII Complexes
  131. Trifluoroethoxy‐Coated Subphthalocyanine affects Trifluoromethylation of Alkenes and Alkynes even under Low‐Energy Red‐Light Irradiation
  132. Construction of Fluorinated Benzoxathiin Skeleton by Successive Perfluorophenylthiolation/Cyclization of Activated α-Methylene Ketones by Perfluorophenyl Diethylaminosulfur Difluoride
  133. Difluoromethylthiolation of Phenols and Related Compounds with a HF2CSO2Na/Ph2PCl/Me3SiCl System
  134. Catalytic Asymmetric 1,3‐Dipolar Cycloaddition of β‐Fluoroalkylated α,β‐Unsaturated 2‐Pyridylsulfones with Nitrones for Chiral Fluoroalkylated Isoxazolidines and γ‐Amino Alcohols
  135. Asymmetric synthesis of α-deuterated α-amino acids
  136. Diastereoselective synthesis of fluoroisosteric analogues of antiparasitic pyrrolobenzoxazine alkaloids from tryptophan by successive fluorination–cyclization and a Meisenheimer-type rearrangement
  137. IF5 affects the final stage of the Cl–F exchange fluorination in the synthesis of pentafluoro-λ6-sulfanyl-pyridines, pyrimidines and benzenes with electron-withdrawing substituents
  138. Induction of human cytochrome P450 3A enzymes in cultured placental cells by thalidomide and relevance to bioactivation and toxicity
  139. SF5-Pyridylaryl-λ3-iodonium salts and their utility as electrophilic reagents to access SF5-pyridine derivatives in the late-stage of synthesis
  140. Silver-induced self-immolative Cl–F exchange fluorination of arylsulfur chlorotetrafluorides: synthesis of arylsulfur pentafluorides
  141. Synthesis of chiral (tetrazolyl)methyl-containing acrylates via silicon-induced organocatalytic kinetic resolution of Morita–Baylis–Hillman fluorides
  142. Perfluoroalkyl Analogues of Diethylaminosulfur Trifluoride: Reagents for Perfluoroalkylthiolation of Active Methylene Compounds under Mild Conditions
  143. Alkynyl Cinchona Catalysts affect Enantioselective Trifluoromethylation for Efavirenz under Metal-Free Conditions
  144. Importance of a Fluorine Substituent for the Preparation of meta‐ and para‐Pentafluoro‐λ6‐sulfanyl‐Substituted Pyridines
  145. Assessment of Protein Binding of 5-Hydroxythalidomide Bioactivated in Humanized Mice with Human P450 3A-Chromosome or Hepatocytes by Two-Dimensional Electrophoresis/Accelerator Mass Spectrometry
  146. Direct Fluoro‐aminosulfenylation of Active Methylenes by Dialkylaminosulfur Trifluorides under Catalyst‐Free Conditions
  147. Asymmetric Desymmetrization via Metal‐Free C−F Bond Activation: Synthesis of 3,5‐Diaryl‐5‐fluoromethyloxazolidin‐2‐ones with Quaternary Carbon Centers
  148. Difluoromethanesulfonyl hypervalent iodonium ylides for electrophilic difluoromethylthiolation reactions under copper catalysis
  149. Novel Use of CF3SO2Cl for the Metal-Free Electrophilic Trifluoromethylthiolation
  150. Organocatalytic Enantioselective Nucleophilic Alkynylation of Allyl Fluorides Affording Chiral Skipped Ene‐ynes
  151. Activation of Trifluoromethylthio Moiety by Appending Iodonium Ylide under Copper Catalysis for Electrophilic Trifluoromethylation Reaction
  152. 2‐Diazo‐1‐phenyl‐2‐((trifluoromethyl)sulfonyl)ethan‐1‐one: Another Utility for Electrophilic Trifluoromethylthiolation Reactions
  153. Methyl NFSI: atom-economical alternative to NFSI shows higher fluorination reactivity under Lewis acid-catalysis and non-catalysis
  154. Design, synthesis and optical properties of unsymmetrical subphthalocyanine trimer connected by phloroglucinol via axial positions
  155. Successive C–C bond cleavage, fluorination, trifluoromethylthio- and pentafluorophenylthiolation under metal-free conditions to provide compounds with dual fluoro-functionalization
  156. Flow trifluoromethylation of carbonyl compounds by Ruppert–Prakash reagent and its application for pharmaceuticals, efavirenz and HSD-016
  157. Synthesis of fluorinated donepezil by palladium-catalyzed decarboxylative allylation of α-fluoro-β-keto ester with tri-substituted heterocyclic alkene and the self-disproportionation of its enantiomers
  158. Enantiomerization of Allylic Trifluoromethyl Sulfoxides Studied by HPLC Analysis and DFT Calculations
  159. Stereoselective Synthesis of β-Lactam-triflones under Catalyst-Free Conditions
  160. Simulation of Human Plasma Concentrations of Thalidomide and Primary 5-Hydroxylated Metabolites Explored with Pharmacokinetic Data in Humanized TK-NOG Mice
  161. Enantioselective Trichloromethylation of MBH‐Fluorides with Chloroform Based on Silicon‐assisted C−F Activation and Carbanion Exchange Induced by a Ruppert–Prakash Reagent
  162. Corrigendum: Regioisomer-Free C 4h β-Tetrakis(tert -butyl)metallo-phthalocyanines: Regioselective Synthesis and Spectral Investigations
  163. Organocatalyzed Trifluoromethylation of Ketones and Sulfonyl Fluorides by Fluoroform under a Superbase System
  164. Synthesis of Phthalocyanines with a Pentafluorosulfanyl Substituent at Peripheral Positions
  165. Difluoromethylation of Terminal Alkynes by Fluoroform
  166. Carbene-Induced Intra- vs Intermolecular Transfer-Fluoromethylation of Aryl Fluoromethylthio Compounds under Rhodium Catalysis
  167. Design, synthesis, spectral investigations and biological activity of fluorinated phthalocyanine conjugated with galactose and comparison to its non-fluorinated counterpart
  168. Synthesis of Diaryliodonium Salts Having Pentafluorosulfanylarenes and Their Application to Electrophilic Pentafluorosulfanylarylation of C-, O-, N-, and S-Nucleophiles
  169. Synthesis of Billard–Langlois Reagents and their Derivatives by Copper‐Catalyzed N‐Trifluoromethylthiolation of Arylamines with a Trifluoromethanesulfonyl Hypervalent Iodonium Ylide
  170. Trifluoromethyl Sulfoxides from Allylic Alcohols and Electrophilic SCF3 Donor by [2,3]-Sigmatropic Rearrangement
  171. Catalytic Trifluoromethylation of Aryl- and Vinylboronic Acids by 2-Cyclopropyl-1-(trifluoromethyl)benzo[b]thiophenium Triflate
  172. Catalytic Asymmetric Synthesis of Enantioenriched Heterocycles Bearing a CCF3 Stereogenic Center
  173. Pentafluorosulfanyl (SF5) in dyes: C3-Regioselective synthesis of α-mono-substituted subphthalocyanine with SF5-phenyl group
  174. Trifluoromethylthiolation of Allylsilanes and Silyl Enol Ethers with Trifluoromethanesulfonyl Hypervalent Iodonium Ylide under Copper Catalysis
  175. Copper-Catalyzed Regioselective Trifluoromethylthiolation of Pyrroles by Trifluoromethanesulfonyl Hypervalent Iodonium Ylide
  176. Self-disproportionation of enantiomers of thalidomide and its fluorinated analogue via gravity-driven achiral chromatography: mechanistic rationale and implications
  177. Synthesis and optical properties of subphthalocyanine homo- and heterodimers axially connected via a hydroquinone linker
  178. Reactions of allyl alcohols and boronic acids with trifluoromethanesulfonyl hypervalent iodonium ylide under copper-catalysis
  179. Synthesis and property of novel phthalocyanine having a 3,5-bis-pentafluorosulfanylphenyl group on the α-peripheral position
  180. Regioisomer-Free C 4h β-Tetrakis(tert -butyl)metallo-phthalocyanines: Regioselective Synthesis and Spectral Investigations
  181. Synthesis and optical properties of trifluoroethoxy-substituted double-decker phthalocyanines
  182. Sterically Demanding Unsymmetrical Diaryl‐λ3‐iodanes for Electrophilic Pentafluorophenylation and an Approach to α‐Pentafluorophenyl Carbonyl Compounds with an All‐Carbon Stereocenter
  183. Synthetic Methods for Compounds Having CF3–S Units on Carbon by Trifluoromethylation, Trifluoromethylthiolation, Triflylation, and Related Reactions
  184. Asymmetric Synthesis of Agrochemically Attractive Trifluoromethylated Dihydroazoles and Related Compounds under Organocatalysis
  185. Studies on the C/O-regioselectivity in Electrophilic Fluoromethylations of β-Ketoesters based on Thermodynamics by Ab initio Calculations
  186. (S)-(Trifluoromethyl)diphenylsulfonium Triflate
  187. Asymmetric Synthesis of Efavirenz via Organocatalyzed Enantioselective Trifluoromethylation
  188. Bis(pentafluorosulfanyl)phenyl Azide as an Expeditious Tool for Click Chemistry toward Antitumor Pharmaceuticals
  189. Thalidomide Increases Human Hepatic Cytochrome P450 3A Enzymes by Direct Activation of the Pregnane X Receptor
  190. Diastereoselective Additive Trifluoromethylation/Halogenation of Isoxazole Triflones: Synthesis of All-Carbon-Functionalized Trifluoromethyl Isoxazoline Triflones
  191. S‐((Phenylsulfonyl)difluoromethyl)thiophenium Salts: Carbon‐Selective Electrophilic Difluoromethylation of β‐Ketoesters, β‐Diketones, and Dicyanoalkylidenes
  192. S‐((Phenylsulfonyl)difluoromethyl)thiophenium Salts: Carbon‐Selective Electrophilic Difluoromethylation of β‐Ketoesters, β‐Diketones, and Dicyanoalkylidenes
  193. Asymmetric Mannich reaction between (S)-N-(tert-butanesulfinyl)-3,3,3-trifluoroacetaldimine and malonic acid derivatives. Stereodivergent synthesis of (R)- and (S)-3-amino-4,4,4-trifluorobutanoic acids
  194. NH-type of chiral Ni(ii) complexes of glycine Schiff base: design, structural evaluation, reactivity and synthetic applications
  195. A phthalocyanine–subphthalocyanine heterodinuclear dimer: comparison of spectroscopic properties with those of homodinuclear dimers of constituting units
  196. Iodoarene-catalyzed fluorination and aminofluorination by an Ar-I/HF·pyridine/mCPBA system
  197. An aza-Michael addition protocol to fluoroalkylated β-amino acid derivatives and enantiopure trifluoromethylated N-heterocycles
  198. Direct nucleophilic difluoromethylation of aromatic isoxazoles activated by electron-withdrawing groups using (difluoromethyl)trimethylsilane
  199. Human Cytochrome P450 Oxidation of 5-Hydroxythalidomide and Pomalidomide, an Amino Analogue of Thalidomide
  200. Kinetic Resolution of Allyl Fluorides by Enantioselective Allylic Trifluoromethylation Based on Silicon‐Assisted CF Bond Cleavage
  201. Redox chemistry of trifluoromethyl sulfonium salts as CF3 radical sources
  202. Regioselective 1,4-trifluoromethylation of α,β-unsaturated ketones via a S-(trifluoromethyl)diphenylsulfonium salts/copper system
  203. Stereoselective Synthesis of Vinyl Triflones and Heteroaryl Triflones through Anionic O→Cvinyl and N→Cvinyl Trifluoromethanesulfonyl Migration Reactions
  204. Enantioselective Synthesis of 5‐Trifluoromethyl‐2‐isoxazolines and Their N‐Oxides by [Hydroxy(tosyloxy)iodo]benzene‐Mediated Oxidative N–O Coupling
  205. Chiral N‐Fluorodibenzenesulfonimide Analogues for Enantioselective Electrophilic Fluorination and Oxidative Fluorination
  206. Cinchona alkaloid/TMAF combination: Enantioselective trifluoromethylation of aryl aldehydes
  207. Highly Enantioselective Monofluoromethylation of C2-Arylindoles Using FBSM under Chiral Phase-Transfer Catalysis
  208. Trifluoromethanesulfonyl Hypervalent Iodonium Ylide for Copper-Catalyzed Trifluoromethylthiolation of Enamines, Indoles, and β-Keto Esters
  209. Phthalocyanine with Trifluoroethoxy Substituents for Organic Solar Cells
  210. Benzenesulfenyl Chloride
  211. Efficient Access to Trifluoromethyl Diarylpyrrolines and their N‐Oxides through Enantioselective Conjugate Addition of Nitromethane to β,β‐Disubstituted Enones
  212. In Vivo Drug Interactions of the Teratogen Thalidomide with Midazolam: Heterotropic Cooperativity of Human Cytochrome P450 in Humanized TK-NOG Mice
  213. SelectiveO-Difluoromethylation of 1,3-Diones by Bromodifluoromethylating Reagents
  214. Remote Anionic Fries Rearrangement of Sulfonates: Regioselective Synthesis of Indole Triflones
  215. Enantioselective Synthesis of Epoxides Having a Tetrasubstituted Trifluoromethylated Carbon Center: Methylhydrazine‐Induced Aerobic Epoxidation of β,β‐Disubstituted Enones
  216. Transition-metal-free oxidative trifluoromethylation of unsymmetrical biaryls with trifluoromethanesulfinate
  217. A sterically demanding organo-superbase avoids decomposition of a naked trifluoromethyl carbanion directly generated from fluoroform
  218. Enantioselective monofluoromethylation of aldehydes with 2-fluoro-1,3-benzodithiole-1,1,3,3-tetraoxide catalyzed by a bifunctional cinchona alkaloid-derived thiourea–titanium complex
  219. Efficient direct ester condensation between equimolar amounts of carboxylic acids and alcohols catalyzed by trifluoromethanesulfonic acid (TfOH) in Solkane365mfc
  220. New Approaches to the Regioselective Synthesis of Heteroaryl Triflones
  221. CF Bond Activation of Unactivated Aliphatic Fluorides: Synthesis of Fluoromethyl‐3,5‐diaryl‐2‐oxazolidinones by Desymmetrization of 2‐Aryl‐1,3‐difluoropropan‐2‐ols
  222. 3,5-Bis(pentafluorosulfanyl)phenylboronic acid: A new organocatalyst for Conia-ene carbocyclization of 1,3-dicarbonyl compounds having terminal alkynes
  223. N-2-Iodobenzylcinchoninium bromide is effective for catalytic enantioselective trifluoromethylation of azomethine imines in Solkane® 365mfc
  224. Decarboxylative Allylation of Trifluoroethyl Sulfones and Approach to Difluoromethyl Compounds
  225. Regioselective Synthesis of Pyrazole Triflones Based on Triflyl Alkyne Cycloadditions
  226. Enantioselective Aza‐Morita–Baylis–Hillman Reactions of Acrylonitrile Catalyzed by Palladium(II) Pincer Complexes having C2‐Symmetric Chiral Bis(imidazoline) Ligands
  227. Design and Photonic Properties of Novel Fluorinated Copolymers Bearing Phthalocyanine Side Groups
  228. Enantioselective Synthesis of AG‐041R by using N‐Heteroarenesulfonyl Cinchona Alkaloid Amides as Organocatalysts
  229. Enantioselective Synthesis of Imidazolines with Quaternary Stereocenters by Organocatalytic Reaction of N-(Heteroarenesulfonyl)imines with Isocyanoacetates
  230. Regioselective Synthesis of Heteroaryl Triflones by LDA (Lithium Diisopropylamide)-Mediated Anionic Thia-Fries Rearrangement
  231. Fundamental Study on Organic Solar Cells Based on Soluble Zinc Phthalocyanine
  232. Organocatalytic Asymmetric Synthesis of Trifluoromethyl‐substituted Diarylpyrrolines: Enantioselective Conjugate Cyanation of β‐Aryl‐β‐trifluoromethyl‐disubstituted Enones
  233. Enantioselective 5‐endo‐dig Carbocyclization of β‐Ketoesters with Internal Alkynes Employing a Four‐Component Catalyst System
  234. Suzuki–Miyaura Cross‐Coupling Reactions in a Solkane365/227/Ethanol Blend at Ambient Temperature
  235. In Vivo Formation of Dihydroxylated and Glutathione Conjugate Metabolites Derived from Thalidomide and 5-Hydroxythalidomide in Humanized TK-NOG Mice
  236. Synthesis of Isoxazole Triflones
  237. Organic base-catalyzed stereodivergent synthesis of (R)- and (S)-3-amino-4,4,4-trifluorobutanoic acids
  238. Partially saturated fluorinated heterocycles: diastereo- and enantioselective synthesis of β-trifluoromethyl-pyrroline carboxylates
  239. Catalytic enantioselective synthesis of β-trifluoromethyl pyrrolines
  240. Efficient synthesis of unsymmetrical S-(bromodifluoromethyl)diarylsulfonium salts for electrophilic bromodifluoromethylating reagents
  241. 5.9 Oxidation: C–X Bond Formation (X=Halogen, S, Se)
  242. Direct Enantioselective Three‐Component Kabachnik–Fields Reaction Catalyzed by Chiral Bis(imidazoline)‐Zinc(II) Catalysts
  243. Enantioselective Reaction of Imines and Benzyl Nitriles Using Palladium Pincer Complexes with C2‐Symmetric Chiral Bis(imidazoline)s
  244. Organocatalytic Enantioselective Decarboxylative Addition of Malonic Acids Half Thioesters to Isatins
  245. A New Synthetic Approach to Efavirenz through Enantioselective Trifluoromethylation by Using the Ruppert–Prakash Reagent
  246. Asymmetric Allylic Monofluoromethylation and Methylation of Morita–Baylis–Hillman Carbonates with FBSM and BSM by Cooperative Cinchona Alkaloid/FeCl2 Catalysis
  247. Synthesis of Indole and Biindolyl Triflones: Trifluoromethanesulfonylation of Indoles with Tf2O/TTBP (2,4,6-tri-tert-butylpyridine) System
  248. Trifluoromethylation of Aromatic Isoxazoles: Regio‐ and Diastereoselective Route to 5‐Trifluoromethyl‐2‐isoxazolines
  249. Construction of Trifluoromethyl‐Bearing Quaternary Carbon Centers by Intramolecular Decarboxylative Allylation of α‐Trifluoromethyl β‐Keto Esters
  250. Organocatalyzed Regio- and Enantioselective Allylic Trifluoromethylation of Morita–Baylis–Hillman Adducts Using Ruppert–Prakash Reagent
  251. Cu-Mediated Chemoselective Trifluoromethylation of Benzyl Bromides Using Shelf-Stable Electrophilic Trifluoromethylating Reagents
  252. ChemInform Abstract: Inherent Oxygen Preference in Enolate Monofluoromethylation and a Synthetic Entry to Monofluoromethyl Ethers.
  253. Fluorothalidomide: A Characterization of Maternal and Developmental Toxicity in Rabbits and Mice
  254. N-Fluoro-(3,5-di-tert-butyl-4-methoxy)benzenesulfonimide (NFBSI): A sterically demanding electrophilic fluorinating reagent for enantioselective fluorination
  255. Robust synthesis of trifluoromethionine and its derivatives by reductive trifluoromethylation of amino acid disulfides by CF3I/Na/Liq.NH3 system
  256. In Vivo Formation of a Glutathione Conjugate Derived from Thalidomide in Humanized uPA-NOG Mice
  257. Catalyst-free and catalytic Friedel–Crafts alkylations of indoles in Solkane® 365mfc, an environmentally benign alternative solvent
  258. Organic reaction in Solkane® 365 mfc: homocoupling reaction of terminal alkynes
  259. Asymmetric synthesis of chiral trifluoromethylated heliotridane via highly catalytic asymmetric Friedel–Crafts alkylation with β-trifluoromethylated acrylates and pyrroles
  260. Influence of new fullerene derivatives with fluorocarbon substituent on performance of polymer solar cells
  261. Inherent Oxygen Preference in Enolate Monofluoromethylation and a Synthetic Entry to Monofluoromethyl Ethers
  262. Asymmetric Synthesis of Both Mirror Images of 3′-Fluorothalidomide by Enantiodivergent Fluorination Using a Single, Cinchona Alkaloid
  263. Poly[(3-hexylthiophene)-block-(3-semifluoroalkylthiophene)] for Polymer Solar Cells
  264. Cinchona Alkaloid-Catalyzed Asymmetric Trifluoromethylation of Alkynyl Ketones with Trimethylsilyl Trifluoromethane
  265. Expeditious Synthesis of Trifluoromethylated Heterocycles: Noncatalytic 1,3-Dipolar Cyclization of Azomethine Imines with (α-Trifluoromethyl)acrylates
  266. Enantioselective Synthesis of Trifluoromethyl‐Substituted 2‐Isoxazolines: Asymmetric Hydroxylamine/Enone Cascade Reaction
  267. Enantioselective Friedel−Crafts Reaction of β-Trifluoromethylated Acrylates with Pyrroles and Its Application to the Synthesis of Trifluorinated Heliotridane
  268. Enantioselective Aldol Reaction using Recyclable Montmorillonite‐Entrapped N‐(2‐Thiophenesulfonyl)prolinamide
  269. Enantioselective desymmetrization of meso-N-(heteroarenesulfonyl)aziridines with TMSN3 catalyzed by chiral Lewis acids
  270. Trifluoroethoxy‐Coating Improves the Axial Ligand Substitution of Subphthalocyanine
  271. Cinchona Alkaloid/TiIV‐Catalyzed Enantioselective Enamine–Trifluoropyruvate Condensation–Cyclization Reaction and Its Application to Drug‐like Heterocycles
  272. Shelf-stable electrophilic trifluoromethylating reagents: A brief historical perspective
  273. Human Liver Microsomal Cytochrome P450 3A Enzymes Involved in Thalidomide 5-Hydroxylation and Formation of a Glutathione Conjugate
  274. Perfluoroisopropyl Zinc Phthalocyanines Conjugated with Deoxyribonucleosides: Synthesis, Photophysical Properties and In Vitro Photodynamic Activities
  275. Solubility of trifluoroethoxyphthalocyanines and -subphthalocyanines in liquid and supercritical carbon dioxide
  276. ChemInform Abstract: Catalytic Enantioselective Hydrophosphonylation of Ketimines Using Cinchona Alkaloids.
  277. Corrigendum to “Cytotoxic effect of amide derivatives of trifluoromethionine against the enteric protozoan parasite Entamoeba histolytica” [Int. J. Antimicrob. Agents 31 (2010) 56–61]
  278. Self-disproportionation of enantiomers of heterocyclic compounds having a tertiary trifluoromethyl alcohol center on chromatography with a non-chiral system
  279. ChemInform Abstract: Solkane® 365mfc Is an Environmentally Benign Alternative Solvent for Trifluoromethylation Reactions.
  280. ChemInform Abstract: Synthesis of Fluorinated Allenes via Palladium‐Catalyzed Monofluoromethylation Using FBSM.
  281. Evaluation of stability difference between asymmetric homochiral dimer in (S)-thalidomide crystal and symmetric heterochiral dimer in (RS)-thalidomide crystal
  282. Synthesis of Benzene-centered Trinuclear Phthalocyanines by Triple-click Chemistry
  283. 2‐Fluoro‐1,3‐benzodithiole‐1,1,3,3‐tetraoxide: A Reagent for Nucleophilic Monofluoromethylation of Aldehydes
  284. Copper‐Catalyzed Enantioselective Three‐Component Synthesis of Optically Active Propargylamines from Aldehydes, Amines, and Aliphatic Alkynes
  285. Enantioselective Friedel−Crafts Reaction of β-Trifluoromethylated Acrylates with Pyrroles and Its Application to the Synthesis of Trifluorinated Heliotridane
  286. Efficient Access to Extended Yagupolskii–Umemoto‐Type Reagents: Triflic Acid Catalyzed Intramolecular Cyclization of ortho‐Ethynylaryltrifluoromethylsulfanes
  287. Asymmetric Syntheses Using Heteroarenesulfonyl Groups as a Highly Functional Protecting-activating Group
  288. Cytotoxic effect of amide derivatives of trifluoromethionine against the enteric protozoan parasite Entamoeba histolytica
  289. Synthesis and Configurational Stability of (S)- and (R)-Deuteriothalidomides
  290. Catalytic Enantioselective Hydrophosphonylation of Ketimines Using Cinchona Alkaloids
  291. Synthesis, photophysical and electrochemical properties of perfluoroisopropyl substituted binuclear phthalocyanine conjugated with a butadiyne linker
  292. Asymmetric synthesis of α-fluoro-α-sulfenyl-β-ketoesters using DBFOX–Ph/Ni(II) complex
  293. Design and Synthesis of Thalidomide–Deoxyribonucleoside Chimeras
  294. Construction of Nonadjacent Stereocenters Containing a Trifluoromethylated Carbon by Organocatalyzed Michael Addition of β-Ketoesters to 2-(Trifluoromethyl)acrylate
  295. Dihydroquinidine Acetate
  296. Dihydroquinine Acetate
  297. A DBFOX‐Ph‐Based Combinatorial Catalyst for Enantioselective Fluorination of Aryl Acetyl and 3‐Butenoyl Thiazolidinones
  298. Catalytic Enantioselective Trifluoromethylation of Azomethine Imines with Trimethyl(trifluoromethyl)silane
  299. Synthesis of novel C2-symmetric chiral crown ethers and their application to enantioselective trifluoromethylation of aldehydes and ketones
  300. First Enantioselective Synthesis of (R)‐Convolutamydine B and E with N‐(Heteroarenesulfonyl)prolinamides
  301. Synthesis, configurational stability and stereochemical biological evaluations of (S)- and (R)-5-hydroxythalidomides
  302. Organocatalytic Enantioselective Aza-Friedel-Crafts Alkylation of Pyrroles with N-(Heteroarenesulfonyl)imines
  303. Dihydroquinidine Acetate
  304. Dihydroquinine Acetate
  305. Synthesis and spectroscopic investigation of trifluoroethoxy-coated phthalocyanine linked with fullerene
  306. Thalidomide protects against ischemic neuronal damage induced by focal cerebral ischemia in mice
  307. New diarylmethanofullerene derivatives and their properties for organic thin-film solar cells
  308. A Dynamic Kinetic Asymmetric Transformation in the α‐Hydroxylation of Racemic Malonates and Its Application to Biologically Active Molecules
  309. Enantioselective electrophilic trifluoromethylation of β-keto esters with Umemoto reagents induced by chiral nonracemic guanidines
  310. Synthesis of fluorinated allenes via palladium-catalyzed monofluoromethylation using FBSM
  311. Solkane® 365mfc is an environmentally benign alternative solvent for trifluoromethylation reactions
  312. Synthesis of trifluoroethoxy-coated binuclear phthalocyanines with click spacers and investigation of their clamshell behaviour
  313. Recent advances in enantioselective trifluoromethylation reactions
  314. Catalytic Enantioselective Michael Addition of 1‐Fluorobis(phenylsulfonyl)methane to α,β‐Unsaturated Ketones Catalyzed by Cinchona Alkaloids
  315. ChemInform Abstract: Fluorinated Johnson Reagent for Transfer‐Trifluoromethylation to Carbon Nucleophiles.
  316. Enantioselective Synthesis of (R)‐Convolutamydine A with New N‐Heteroarylsulfonylprolinamides
  317. ChemInform Abstract: Recent Advances in Enantioselective Trifluoromethylation Reactions
  318. Novel Enantiocomplementary C2‐Symmetric Chiral Bis(imidazoline) Ligands: Highly Enantioselective Friedel–Crafts Alkylation of Indoles with Ethyl 3,3,3‐Trifluoropyruvate
  319. Fluorinated Johnson Reagent for Transfer‐Trifluoromethylation to Carbon Nucleophiles
  320. Catalytic and Highly Enantioselective Reactions of α‐Sulfonyl Carbanions with Chiral Bis(oxazoline)s
  321. Organocatalytic Enantioselective Hydrophosphonylation of Sulfonylimines having a Heteroarenesulfonyl Group as a Novel Stereocontroller
  322. DBFOX-Ph/metal complexes: Evaluation as catalysts for enantioselective fluorination of 3-(2-arylacetyl)-2-thiazolidinones
  323. Cinchona Alkaloid Catalyzed Enantioselective Fluorination of Allyl Silanes, Silyl Enol Ethers, and Oxindoles
  324. Enantioselective CC Bond Formation to Sulfonylimines through Use of the 2‐Pyridinesulfonyl Group as a Novel Stereocontroller
  325. Enzymatic resolution and evaluation of enantiomers of cis-5′-hydroxythalidomide
  326. Synthesis of covalently linked binuclear clamshell phthalocyanine by double-click reaction
  327. Synthesis and properties of trifluoroethoxy-coated binuclear phthalocyanine
  328. Highly Enantioselective Reactions of Configurationally Labile Epimeric Diamine Complexes of Lithiated S‐Benzyl Thiocarbamates
  329. Desymmetrization‐like Catalytic Enantioselective Fluorination of Malonates and Its Application to Pharmaceutically Attractive Molecules
  330. Asymmetric lithiation of 2-alkynyl aryl sulfides—Enantio- and diastereoselective formation of allenyl aryl sulfides and their application in nickel-catalyzed cross-coupling reactions
  331. Cinchona‐Alkaloid‐Catalyzed Enantioselective Direct Aldol‐Type Reaction of Oxindoles with Ethyl Trifluoropyruvate
  332. Highly Enantioselective Reactions of α‐Sulfonyl Carbanions of Trifluoromethyl Sulfones
  333. Ammonium bromides/KF catalyzed trifluoromethylation of carbonyl compounds with (trifluoromethyl)trimethylsilane and its application in the enantioselective trifluoromethylation reaction
  334. Cinchona Alkaloids/TMAF Combination-Catalyzed Nucleophilic Enantioselective Trifluoromethylation of Aryl Ketones
  335. DNA‐Mediated Enantioselective Carbon—Fluorine Bond Formation
  336. Enantioselective Mannich-type reaction of sulfonylimines having 2-pyridylsulfonyl group as a novel stereocontroller
  337. New approaches to enantioselective fluorination: Cinchona alkaloids combinations and chiral ligands/metal complexes
  338. Cinchona Alkaloid-Catalyzed Enantioselective Monofluoromethylation Reaction Based on Fluorobis(phenylsulfonyl)methane Chemistry Combined with a Mannich-type Reaction
  339. DNA-Mediated Enantioselective Carbon-Fluorine Bond Formation
  340. Synthesis and Spectral Properties of a Deoxyribose-Phthalocyanine ­Conjugate Using a Sonogashira Coupling Reaction
  341. Design, Synthesis, and Spectroscopic Investigation of Zinc Dodecakis(trifluoroethoxy)phthalocyanines Conjugated with Deoxyribonucleosides
  342. Efficient Synthesis of Bicyclic α-Hydroxy-α-trifluoromethyl-γ-lactams
  343. Lewis Acid-Catalyzed Enantioselective Hydroxylation Reactions of Oxindoles and β-Keto Esters Using DBFOX Ligand
  344. Enantioselective Strecker-type reaction to sulfonylimines having a 2-pyridylsulfonyl group as a novel stereocontroller
  345. Enantioselective Fluorination Mediated by Cinchona Alkaloids/Selectfluor Combinations: A Catalytic Approach.
  346. Fluorobis(phenylsulfonyl)methane: A Fluoromethide Equivalent and Palladium‐Catalyzed Enantioselective Allylic Monofluoromethylation
  347. Enantioselective fluorination mediated by cinchona alkaloids/selectfluor combinations: A catalytic approach
  348. Remote asymmetric trifluoromethylation induced by chiral sulfinyl group: synthesis of enantiomerically pure 1-(2-naphthyl)-2,2,2-trifluoroethanol
  349. Lewis acid-catalyzed tri- and difluoromethylation reactions of aldehydes
  350. Tri-tert-butylphosphine is an Efficient Promoter for the Trifluoromethylation Reactions of Aldehydes, Ketones, Imides and Imines
  351. Enantioselective nucleophilic addition to N-(2-pyridylsulfonyl)imines by use of dynamically induced chirality
  352. Highly Enantioselective Catalytic Fluorination and Chlorination Reactions of Carbonyl Compounds Capable of Two‐Point Binding
  353. Cinchona Alkaloid/Sulfinyl Chloride Combinations. Enantioselective Sulfinylating Agents of Alcohols.
  354. Cinchona Alkaloid/Sulfinyl Chloride Combinations:  Enantioselective Sulfinylating Agents of Alcohols [J. Am. Chem. Soc. 2005, 127, 1374−1375].
  355. Cinchona Alkaloid/Sulfinyl Chloride Combinations:  Enantioselective Sulfinylating Agents of Alcohols
  356. Cinchona Alkaloid-Sulfinyl Chloride Combinations: Catalytic Enantio­selective Sulfinylation of Alcohols
  357. Enantioselective synthesis of chiral sulfinates using chiral diamines
  358. Asymmetric Synthesis of Axially Chiral cis-Arylmethylenebicyclo[3.3.0]octanes Using α-Thio- and α-Selenoorganolithium Compounds
  359. First Enantio‐Flexible Fluorination Reaction Using Metal‐Bis(oxazoline) Complexes.
  360. 20-Deoxy-20-fluorocamptothecin: Design and Synthesis of Camptothecin Isostere
  361. Chiral discrimination between thalidomide enantiomers using a solid surface with two-dimensional chirality
  362. Enantioselective Fluorination Mediated by N-Fluoroammonium Salts of Cinchona Alkaloids:  First Enantioselective Synthesis of BMS-204352 (MaxiPost)
  363. ChemInform Abstract: Synthesis of Nonpolar Peptide Nucleic Acid Monomers Containing Fluoroaromatics.
  364. Enantioselective Fluorination Mediated by Cinchona Alkaloid Derivatives/Selectfluor Combinations:  Reaction Scope and Structural Information forN-Fluorocinchona Alkaloids
  365. A Fundamentally New Approach to Enantioselective Fluorination Based on Cinchona Alkaloid Derivatives/Selectfluor Combination
  366. Novel Methods for the Facile Construction of 3,3-Disubstituted and 3,3-Spiro-2H,4H-benzo[e]1,2-thiazine-1,1-diones:  Synthesis of (11S,12R,14R)-2-Fluoro-14-methyl-11-(methylethyl)spiro[4H-benzo[e]...
  367. ChemInform Abstract: (R)‐ and (S)‐3‐Fluorothalidomides: Isosteric Analogues of Thalidomide.
  368. Application of the Ugi four-component condensation reaction for the synthesis of α,α- and α,β-dipeptides substituted with fluoroarylalkyl pendent groups†
  369. N-Fluoro-3-cyclohexyl-3-methyl-2,3- dihydrobenzo[1,2-d]isothiazole 1,1-Dioxide:  An Efficient Agent for Electrophilic Asymmetric Fluorination of Enolates
  370. ChemInform Abstract: Research on the Correlation Between the Pummerer Reaction and Penicillin Biosynthesis
  371. Synthesis of γ-fluoro-α-methyl-α-amino acids. A new alkylation procedure for ester imines
  372. Structure of isopenicillinN synthase complexed with substrate and the mechanism ofpenicillin formation
  373. Resin-bound peptide libraries showing specific metal ion binding
  374. An expeditious synthesis of (2R,3S)-3-tert-butoxycarbonylamino-1-isobutylamino-4-phenyl-2-butanol, a key building block of HIV protease inhibitors
  375. Highly asymmetric Pummerer-type reaction induced by ethoxy vinyl esters
  376. Electrophilic sulfenylation in a stereocontrolled synthesis of protected (2R,3R)-3-mercaptoaspartic acid from -aspartic acid
  377. Adipoyl-6-aminopenicillanic acid is a substrate for deacetoxycephalosporin C synthase (DAOCS)
  378. A highly asymmetric Pummerer-type cyclization of chiral, non-racemic β-amidosulfoxides induced by O-silylated ketene acetals
  379. A novel diastereoselective synthesis of chiral, non-racemic unsymmetrical thioacetals using silicon-induced Pummerer-type reaction
  380. Enantioselective pummerer-type rearrangement by reaction of O-silylated ketene acetal with enantiopure α-substituted sulfoxides
  381. Pummerer-type Cyclization of Arnstein Tripeptide Analogs Induced by O-Silylated Ketene Acetals: Studies of Penicillin Biosynthesis
  382. A novel asymmetric pummerer reaction induced by ethoxy vinyl ester
  383. Mechanistic studies of Pummerer reaction in acyclic sulfoxides induced by O-silylated ketene acetals
  384. The first highly asymmetric pummerer-type reaction in chiral acyclic sulfoxides: Chemistry of O-silylated ketene acetals
  385. A Novel Method for the Alkoxylation of Azetidin-2-ones at the 4-Position.
  386. An Efficient Synthesis of 4-Heterofunction-Substituted 3-(1-Hydroxy)ethylazetidin-2-ones from 3-(1-Hydroxy)ethyl-4-phenylsulfinylazetidin-2-one by Reaction with Silylated Heteronucleophiles.
  387. Chemistry of O-Silylated Ketene Acetals: A Stereoselective Synthesis of Optically Active Carbapenem Antibiotics, (+)-Thienamycin and (+)-PS-5.
  388. A novel substitution reaction of 4-sulfinylazetidin-2-one with silylated heteronucleophiles: an efficient synthesis of 4-heterofunction substituted 3-(1-hydroxy)ethylazetidin-2-ones
  389. Chemistry of O-Silylated Ketene Acetals: A Mild and Convenient Synthesis of .BETA.-Lactam Antibiotics.
  390. Chemistry of O-silylated ketene acetals: a stereoselective synthesis of chiral thienamycin intermediate
  391. Chemistry of O-silylated ketene acetals: A novel intramolecular Pummerer-type reaction of .OMEGA.-carbamoylsulfoxides leading to .ALPHA.-thiolactams.
  392. Chemistry of O -silylated ketene acetals: Biomimetic synthesis of cis -β-lactams
  393. Novel transformation of azabicyclothionocarbonate to azaspirolactone.
  394. Synthesis of Thalidomide