All Stories

  1. Total Synthesis of (−)-Enigmazole A by the Macrocyclization/Transannular Pyran Cyclization Strategy
  2. Atomic-resolution structure analysis inside an adaptable porous framework
  3. Total Synthesis of (−)-Enigmazole B
  4. Total Synthesis of Marine Macrolide Natural Products by the Macrocyclization/Transannular Pyran Cyclization Strategy
  5. Total Synthesis of (+)-Muricatetrocin B via a Late-Stage Co-Catalyzed Hartung–Mukaiyama Cyclization
  6. An 11-Step Synthesis of (+)-Neopeltolide by the Macrocyclization/Transannular Pyran Cyclization Strategy
  7. Collective Asymmetric Total Synthesis of Cylindricines
  8. Collective Asymmetric Total Synthesis of Cylindricines
  9. N-Terminal-selective Cu-catalyzed [3+2] cycloaddition for irreversible assembly of two modules with a peptide
  10. Au-catalyzed stereodivergent synthesis of 2,5-disubstituted pyrrolidines: total synthesis of (+)-monomorine I and (+)-indolizidine 195B
  11. GIAO NMR Calculation-driven Stereochemical Assignment of Marine Macrolide Natural Products: Assessment of the Performance of DP4 and DP4+ Analyses and Assignment of the Relative Configuration of Leptolyngbyalide A–C/Oscillariolide Macrolactone
  12. Stereoselective Tandem Synthesis of Pyrrolidine Derivatives under Gold Catalysis: An Asymmetric Synthesis of (−)-Lepadiformine A
  13. Total Synthesis of (+)-Neopeltolide by the Macrocyclization/Transannular Pyran Cyclization Strategy
  14. Frontispiece: Tandem Macrolactone Synthesis: Total Synthesis of (−)‐Exiguolide by a Macrocyclization/Transannular Pyran Cyclization Strategy
  15. Frontispiz: Tandem Macrolactone Synthesis: Total Synthesis of (−)‐Exiguolide by a Macrocyclization/Transannular Pyran Cyclization Strategy
  16. Gambierol Blocks a K+ Current Fraction without Affecting Catecholamine Release in Rat Fetal Adrenomedullary Cultured Chromaffin Cells
  17. Tandem Macrolactone Synthesis: Total Synthesis of (−)‐Exiguolide by a Macrocyclization/Transannular Pyran Cyclization Strategy
  18. Tandem Macrolactone Synthesis: Total Synthesis of (−)‐Exiguolide by a Macrocyclization/Transannular Pyran Cyclization Strategy
  19. Determination of the toxicity equivalency factors for ciguatoxins using human sodium channels
  20. Total Synthesis of (−)-Exiguolide, a Potent Anticancer Marine Macrolide
  21. Asymmetric Synthesis of (−)-Atorvastatin Calcium by Tandem Catalysis
  22. Synthesis-Driven Stereochemical Assignment of Marine Polycyclic Ether Natural Products
  23. Stereoselective Synthesis of the Southern Hemisphere Acyclic Domain of Neaumycin B
  24. Ruthenium-Catalyzed Intramolecular Double Hydrofunctionalization of Alkynes. Synthesis of Spirocyclic Hemiaminal Ethers and Their Lewis Acid-Mediated Cleavage/Nucleophilic Addition
  25. Cobalt-Catalyzed Hartung–Mukaiyama Cyclization of γ-Hydroxy Olefins: Stereocontrolled Synthesis of the Tetrahydrofuran Moiety of Amphidinolide N
  26. Total synthesis and complete configurational assignment of amphirionin-2
  27. Structure determination, correction, and disproof of marine macrolide natural products by chemical synthesis
  28. Unified Total Synthesis of (−)‐Enigmazole A and (−)‐15‐ O ‐Methylenigmazole A
  29. Tandem Three‐Component Synthesis of syn ‐1,2‐ and syn ‐1,3‐Diol Derivatives
  30. Total Synthesis of a Marine Macrolide Natural Product, Iriomoteolide-2a: The Fundamental Role of Total Synthesis in Natural Product Chemistry
  31. Cover Feature: Total Synthesis, Stereochemical Revision, and Biological Assessment of Iriomoteolide‐2a (Chem. Eur. J. 36/2019)
  32. Total Synthesis, Stereochemical Revision, and Biological Assessment of Iriomoteolide‐2a
  33. Stereoselective Tandem Synthesis of syn-1,3-Diol Derivatives by Integrating Olefin Cross-Metathesis, Hemiacetalization, and Intramolecular Oxa-Michael Addition
  34. Fluorescence-labeled neopeltolide derivatives for subcellular localization imaging
  35. Ruthenium-Catalyzed Intramolecular Double Hydroalkoxylation of Internal Alkynes
  36. Total Synthesis of (−)-Enigmazole A
  37. Total Synthesis of (−)-Enigmazole A
  38. Total Synthesis and Stereochemical Revision of Iriomoteolide-2a
  39. Total Synthesis and Stereochemical Revision of Iriomoteolide-2a
  40. A Synthetic Analogue of Neopeltolide, 8,9-Dehydroneopeltolide, Is a Potent Anti-Austerity Agent against Starved Tumor Cells
  41. Tetracyclic Truncated Analogue of the Marine Toxin Gambierol Modifies NMDA, Tau, and Amyloid β Expression in Mice Brains: Implications in AD Pathology
  42. Exploiting Ruthenium Carbene-Catalyzed Reactions in Total Synthesis of Marine Oxacyclic Natural Products
  43. Diastereoselective Ring-Closing Metathesis as a Means to Construct Medium-Sized Cyclic Ethers: Application to the Synthesis of a Photoactivatable Gambierol Derivative
  44. Effect of carbon chain length in acyl coenzyme A on the efficiency of enzymatic transformation of okadaic acid to 7- O -acyl okadaic acid
  45. Total Synthesis and Complete Stereostructure of a Marine Macrolide Glycoside, (−)-Lyngbyaloside B
  46. Toward the Total Synthesis of Amphidinolide N: Synthesis of the C8–C29 Fragment
  47. Complete Stereochemical Assignment of Campechic Acids A and B
  48. Contemporary Strategies for the Synthesis of Tetrahydropyran Derivatives: Application to Total Synthesis of Neopeltolide, a Marine Macrolide Natural Product
  49. Progress toward the Total Synthesis of Goniodomin A: Stereocontrolled, Convergent Synthesis of the C12–C36 Fragment
  50. Concise synthesis of the C15–C38 fragment of okadaic acid, a specific inhibitor of protein phosphatases 1 and 2A
  51. Evaluation of gambierol and its analogs for their inhibition of human Kv1.2 and cytotoxicity
  52. Concise synthesis of the A/BCD-ring fragment of gambieric acid A
  53. Studies toward the Total Synthesis of Amphidinolide N: Stereocontrolled Synthesis of the C13–C29 Segment
  54. Concise Synthesis of the C15–C38 Fragment of Okadaic Acid: Application of the Suzuki–Miyaura Reaction to Spiroacetal Synthesis
  55. Programmed Cell Death Induced by (−)-8,9-Dehydroneopeltolide in Human Promyelocytic Leukemia HL-60 Cells under Energy Stress Conditions
  56. Total Synthesis, Stereochemical Reassignment, and Biological Evaluation of (−)-Lyngbyaloside B
  57. Potassium currents inhibition by gambierol analogs prevents human T lymphocyte activation
  58. Total Synthesis and Complete Structural Assignment of Gambieric Acid A, a Large Polycyclic Ether Marine Natural Product
  59. Synthesis and biological evaluation of (+)-neopeltolide analogues: Importance of the oxazole-containing side chain
  60. Stereoselective Synthesis of Medium-Sized Cyclic Ethers: Application of C-Glycosylation Chemistry to Seven- to Nine-Membered Lactone-Derived Thioacetals and Their Sulfone Counterparts
  61. Total Synthesis and Structure Revision of Didemnaketal B
  62. Synthesis and Biological Evaluation of Aspergillide A/Neopeltolide Chimeras
  63. Total Synthesis of the Proposed Structure of Didemnaketal B
  64. Concise Synthesis and Biological Assessment of (+)-Neopeltolide and a 16-Member Stereoisomer Library of 8,9-Dehydroneopeltolide: Identification of Pharmacophoric Elements
  65. Total Synthesis and Biological Evaluation of (+)-Gambieric Acid A and Its Analogues
  66. Total Synthesis of 13-Demethyllyngbyaloside B
  67. Total synthesis and biological evaluation of (−)-exiguolide analogues: importance of the macrocyclic backbone
  68. Stereoselective Synthesis of the C1–C16 Fragment of Goniodomin A
  69. Effect of Gambierol and Its Tetracyclic and Heptacyclic Analogues in Cultured Cerebellar Neurons: A Structure–Activity Relationships Study
  70. Total Synthesis and Complete Stereostructure of Gambieric Acid A
  71. Design and Synthesis of Skeletal Analogues of Gambierol: Attenuation of Amyloid-β and Tau Pathology with Voltage-Gated Potassium Channel andN-Methyl-d-aspartate Receptor Implications
  72. Tandem catalysis in domino olefin cross-metathesis/intramolecular oxa-conjugate cyclization: concise synthesis of 2,6-cis-substituted tetrahydropyran derivatives
  73. A CONCISE SYNTHESIS OF THE AB-RING FRAGMENT OF (−)-GAMBIEROL
  74. Total Synthesis of Tetrahydropyran-Containing Natural Products Exploiting Intramolecular Oxa-Conjugate Cyclization
  75. Stereoselective Synthesis of 2,6-Cis-Substituted Tetrahydropyrans: Brønsted Acid-Catalyzed Intramolecular Oxa-Conjugate Cyclization of α,β-Unsaturated Ester Surrogates
  76. Total Synthesis of (−)-Brevenal: A Streamlined Strategy for Practical Synthesis of Polycyclic Ethers
  77. Studies toward the total synthesis of gambieric acids, potent antifungal polycyclic ethers: convergent synthesis of a fully elaborated GHIJ-ring fragment
  78. A new strategy for the synthesis of substituted dihydropyrones and tetrahydropyrones via palladium-catalyzed coupling of thioesters
  79. Comparative Cytotoxicity of Gambierol versus Other Marine Neurotoxins
  80. Biosynthesis-Inspired Intramolecular Oxa-Conjugate Cyclization of α,β-Unsaturated Thioesters: Stereoselective Synthesis of 2,6-cis-Substituted Tetrahydropyrans
  81. A Convergent Synthesis of the C1−C16 Segment of Goniodomin A via Palladium-Catalyzed Organostannane−Thioester Coupling
  82. Total Synthesis and Biological Assessment of (−)‐Exiguolide and Analogues
  83. Suppression of Colon Cancer Metastasis by Aes through Inhibition of Notch Signaling
  84. Studies toward the total synthesis of gambieric acids: convergent synthesis of the GHIJ-ring fragment having a side chain
  85. Synthetic studies on goniodomin A: convergent assembly of the C15–C36 segment via palladium-catalyzed organostannane–thioester coupling
  86. Total Synthesis of Structurally Complex Marine Oxacyclic Natural Products
  87. Palladium-Catalyzed Synthesis of N- and O-Heterocycles Starting from Enol Phosphates
  88. Convergent Assembly of the Spiroacetal Subunit of Didemnaketal B
  89. The marine polyether gambierol enhances muscle contraction and blocks a transient K+ current in skeletal muscle cells
  90. An enantioselective total synthesis of aspergillides A and B
  91. Studies toward the Total Synthesis of Gambieric Acids: Stereocontrolled Synthesis of a DEFG-Ring Model Compound
  92. A Unified Total Synthesis of Aspergillides A and B
  93. Stereoselective Synthesis of Substituted Tetrahydropyrans via Domino Olefin Cross-Metathesis/Intramolecular Oxa-Conjugate Cyclization
  94. An Efficient Synthesis of 2,6-Disubstituted 2,3-Dihydro-4H-pyran-4-ones via Sonogashira Coupling of p-Toluenethiol Esters
  95. A Concise Total Synthesis of (+)-Neopeltolide
  96. Total Synthesis of (−)-Exiguolide
  97. Highly efficient synthesis of medium-sized lactones via oxidative lactonization: concise total synthesis of isolaurepan
  98. A Concise Total Synthesis of (±)-Centrolobine
  99. Calcium oscillations induced by gambierol in cerebellar granule cells
  100. Total Synthesis and Biological Evaluation of (+)-Neopeltolide and Its Analogues
  101. Toward the Total Synthesis of Goniodomin A, An Actin-Targeting Marine Polyether Macrolide: Convergent Synthesis of the C15−C36 Segment
  102. Stereocontrolled Synthesis of the DEFG-ring Skeleton of Gambieric Acids
  103. Proteomic Analysis Reveals Multiple Patterns of Response in Cells Exposed to a Toxin Mixture
  104. Synthetic Studies on Gambieric Acids, Potent Antifungal Polycyclic Ether Natural Products: Reassignment of the Absolute Configuration of the Nonacyclic Polyether Core by NMR Analysis of Model Compounds
  105. Synthesis of 2-Substituted Indoles and Indolines via Suzuki−Miyaura Coupling/5-endo-trigCyclization Strategies
  106. A New Method for the Generation of Indole-2,3-quinodimethanes from Allenamides
  107. Total Synthesis of (+)-Neopeltolide
  108. An Efficient Strategy for the Synthesis of Endocyclic Enol Ethers and Its Application to the Synthesis of Spiroacetals
  109. Stereocontrolled Synthesis of the A/B-Ring Fragment of Gambieric Acid B: Reassignment of the Absolute Configuration of the Polycyclic Ether Region
  110. Total Synthesis of (−)-Brevenal: A Concise Synthetic Entry to the Pentacyclic Polyether Core
  111. Convergent strategies for the total synthesis of polycyclic ether marine metabolites
  112. Strategies for the Synthesis of 2-Substituted Indoles and Indolines Starting from Acyclic α-Phosphoryloxy Enecarbamates
  113. Divergent Synthesis of Multifunctional Molecular Probes To Elucidate the Enzyme Specificity of Dipeptidic γ-Secretase Inhibitors
  114. An efficient method for the synthesis of enol ethers and enecarbamates. Total syntheses of isoindolobenzazepine alkaloids, lennoxamine and chilenine
  115. A new method for the generation of indole-2,3-quinodimethanes and 2-(N-alkoxycarbonylamino)-1,3-dienes. Intramolecular Heck/Diels–Alder cycloaddition cascade starting from acyclic α-phosphono enecarbamates
  116. A strategy for the synthesis of 2,3-disubstituted indoles starting from N-(o-halophenyl)allenamides
  117. Total Synthesis, Structure Revision, and Absolute Configuration of (−)-Brevenal
  118. Synthesis of biotinylated photoaffinity probes based on arylsulfonamide γ-secretase inhibitors
  119. Synthesis of the JK/LM-ring model of prymnesins, potent hemolytic and ichthyotoxic polycyclic ethers isolated from the red tide alga Prymnesium parvum: confirmation of the relative configuration of the K/L-ring juncture
  120. Total Synthesis of the Proposed Structure of Brevenal
  121. Novel γ-secretase inhibitors discovered by library screening of in-house synthetic natural product intermediates
  122. Effect of Ciguatoxin 3C on Voltage-Gated Na+ and K+ Currents in Mouse Taste Cells
  123. C-terminal Fragment of Presenilin Is the Molecular Target of a Dipeptidic γ-Secretase-specific Inhibitor DAPT (N-[N-(3,5-Difluorophenacetyl)-L-alanyl]-S-phenylglycinet-Butyl Ester)
  124. Synthetic studies on 3-arylquinazolin-4-ones: intramolecular nucleophilic aromatic substitution reaction of 2-carboxamido-3-arylquinazolin-4-ones and its application to the synthesis of secondary aryl amines
  125. Inhibition of Voltage-Gated Potassium Currents by Gambierol in Mouse Taste Cells
  126. Diverted Total Synthesis and Biological Evaluation of Gambierol Analogues: Elucidation of Crucial Structural Elements for Potent Toxicity
  127. Total Synthesis of Polycyclic Ether Natural Products Based on Suzuki-Miyaura Cross-Coupling
  128. Convergent synthesis of the ABCDE ring fragment of ciguatoxins
  129. Synthetic studies on antascomicin A: construction of the C18–C34 fragment
  130. Highly efficient synthesis of medium-sized lactams via intramolecular Staudinger–aza-Wittig reaction of ω-azido pentafluorophenyl ester: synthesis and biological evaluation of LY411575 analogues
  131. Pathological effects on mice by gambierol, possibly one of the ciguatera toxins
  132. Synthesis and biological evaluation of gambierol analogues
  133. Total Synthesis of (−)-Gambierol
  134. Synthetic Studies toward Gambierol. Convergent Synthesis of the Octacyclic Polyether Core