All Stories

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