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  1. The title describes the interaction of a potent antitumor natural compound
  2. The title describes the main work of the article
  3. Stereoselective Allylstannane Addition for a Convergent Synthesis of a Complex Molecule
  4. ChemInform Abstract: Phormidolides B (I) and C (II), Cytotoxic Agents from the Sea: Enantioselective Synthesis of the Macrocyclic Core.
  5. ChemInform Abstract: Addition of Vinylmetallic Reagents to Chiral 2-Formyltetrahydrofuran.
  6. The Larock Reaction in the Synthesis of Heterocyclic Compounds
  7. Inside Cover: Phormidolides B and C, Cytotoxic Agents from the Sea: Enantioselective Synthesis of the Macrocyclic Core (Chem. Eur. J. 1/2015)
  8. Addition of Vinylmetallic Reagents to Chiral 2-Formyltetrahydrofuran
  9. Phormidolides B and C, Cytotoxic Agents from the Sea: Enantioselective Synthesis of the Macrocyclic Core
  10. ChemInform Abstract: Thiopeptide Engineering: A Multidisciplinary Effort Towards Future Drugs
  11. Chiral Thiazoline and Thiazole Building Blocks for the Synthesis of Peptide- Derived Natural Products
  12. Engineering von Thiopeptiden: ein multidisziplinärer Weg zu neuen Wirkstoffen
  13. Thiopeptide Engineering: A Multidisciplinary Effort towards Future Drugs
  14. Dissecting the Structure of Thiopeptides: Assessment of Thiazoline and Tail Moieties of Baringolin and Antibacterial Activity Optimization
  15. Thiopeptide Antibiotics: Retrospective and Recent Advances
  16. From 2,6-Dichloronicotinic Acid to Thiopeptide Cores
  17. ChemInform Abstract: Tetrahydrofuran-Containing Macrolides: A Fascinating Gift from the Deep Sea
  18. Total Synthesis and Stereochemical Assignment of Baringolin
  19. Total Synthesis and Stereochemical Assignment of Baringolin
  20. Tetrahydrofuran-Containing Macrolides: A Fascinating Gift from the Deep Sea
  21. Orthogonal Protecting Groups in the Synthesis of Tryptophanyl-Hexahydropyrroloindoles
  22. Highly efficient, multigram and enantiopure synthesis of (S)-2-(2,4′-bithiazol-2-yl)pyrrolidine
  23. ChemInform Abstract: Structure, Bioactivity and Synthesis of Natural Products with Hexahydropyrrolo[2,3-b]indole
  24. Structure, Bioactivity and Synthesis of Natural Products with Hexahydropyrrolo[2,3-b]indole
  25. Progress on lamellarins
  26. First enantioselective synthesis of isagarin, a natural product isolated from Pentas longiflora Oliv.
  27. ChemInform Abstract: Synthesis of 1,2-Dihydropyrrolo[1,2-c]pyrimidin-1-ones.
  28. ChemInform Abstract: Synthesis of 3-Aryl- and 3-Heteroaryl-7-azaindoles.
  29. ChemInform Abstract: Syntheses of Batzelline A, Batzelline B, Isobatzelline A, and Isobatzelline B.
  30. ChemInform Abstract: Synthesis of Ascididemine and an Isomer.
  31. ChemInform Abstract: Cyclic Ureas as ortho Directing Substituents.
  32. ChemInform Abstract: Ellipticine, Uleine, Apparicine, and Related Alkaloids.
  33. ChemInform Abstract: Synthesis of 5-Arylpyrrolo[1,2-c]pyrimidin-1(2H)-ones.
  34. The Sea as a Source of New Drugs
  35. ChemInform Abstract: Amino Acid-Protecting Groups
  36. Optical Tweezers Study of Topoisomerase Inhibition
  37. Synthesis of the pyrrolo[2,3-c]carbazole core of the dictyodendrins
  38. 1,2-Dimethylindole-3-sulfonyl (MIS) as protecting group for the side chain of arginine
  39. Synthesis of Natural Product Derivatives Containing 2,4‐Concatenated Oxazoles
  40. Phenyl-EDOTn derivatives as super acid labile carboxylic acid protecting groups for peptide synthesis
  41. Advances in Solid-Phase Cycloadditions for Heterocyclic Synthesis
  42. Novel Synthesis of Arylethynyl Heterocycles.
  43. Preparation of penta-azole containing cyclopeptides: challenges in macrocyclization
  44. EDOTn and MIM, new peptide backbone protecting groups
  45. Regioselective Monobromination of Free and Protected Phenols.
  46. Lamellarins: Isolation, Activity and Synthesis
  47. Synthesis of IB-01211, a Cyclic Peptide Containing 2,4-Concatenated Thia- and Oxazoles, via Hantzsch Macrocyclization.
  48. Advances in Solid-Phase Cycloadditions for Heterocyclic Synthesis
  49. Novel Synthesis of Arylethynyl Heterocycles
  50. Solid-Phase Synthesis of Oxathiocoraline by a Key Intermolecular Disulfide Dimer
  51. Regioselective Monobromination of Free and Protected Phenols
  52. Fmoc-2-mercaptobenzothiazole, for the introduction of the Fmoc moiety free of side-reactions
  53. Total Solid-Phase Synthesis of the Azathiocoraline Class of Symmetric Bicyclic Peptides
  54. Solid-Phase Chemistry in the Total Synthesis of Non-Peptidic Natural Products
  55. Modular Total Synthesis of Lamellarin D (I).
  56. Solid-Phase Chemistry in the Total Synthesis of Non-Peptidic Natural Products
  57. Directly Linked Polyazoles: Important Moieties in Natural Products
  58. Semipermanent p-nitrobenzyloxycarbonyl (pNZ) protection of Orn and Lys side chains: prevention of undesired α-Fmoc removal and application to the synthesis of cyclic peptides
  59. Use of p-nitrobenzyloxycarbonyl (pNZ) as a permanent protecting group in the synthesis of Kahalalide F analogs
  60. Modular Total Synthesis of Lamellarin D
  61. A New Approach to 3-Hydroxyquinoline-2-carboxylic Acid.
  62. Chloromethoxymethyl Polystyrene (CMM Resin), an Acid Labile Resin for Anchoring/Cleavage of N-Heterocycles and Oxygen Aromatic Compounds
  63. 5,6-Dihydropyrrolo[2,1-b]isoquinolines as scaffolds for synthesis of lamellarin analogues
  64. A new approach to 3-hydroxyquinoline-2-carboxylic acid
  65. Directly Linked Polyazoles: Important Moieties in Natural Products
  66. Chapter 1 Lamellarins: Isolation, activity and synthesis
  67. Synthesis of Polyheterocyclic Nitrogen-Containing Marine Natural Products.
  68. Solid-phase synthesis of lamellarins Q and O
  69. Solid-phase synthesis of 4H-2-(3-hydroxy-4-methoxyphenyl)-naphtho[1,2-b]pyran-1-one
  70. Gaining diversity in solid-phase synthesis by modulation of cleavage conditions from hydroxymethyl-based supports. Application to lamellarin synthesis
  71. Total Syntheses of Variolin B (Ia) and Deoxyvariolin B (Ib).
  72. Solid-Phase Syntheses of Furopyridine and Furoquinoline Systems
  73. A Combination of Different Spectroscopic Techniques to Monitor the“in situ” Solid-phase Synthesis of Organic Molecules
  74. Total Syntheses of Variolin B and Deoxyvariolin B 1
  75. Synthesis of Variolin B.
  76. Synthesis of variolin B
  77. Solid-Phase Total Synthesis of the Pentacyclic System Lamellarins U and L†
  78. Solid Phase Synthesis of Lamellarins
  79. Synthesis of 5-arylpyrrolo[1,2-c]pyrimidin-1(2H)-ones
  80. ChemInform Abstract: Synthesis of Deoxyvariolin B.
  81. ChemInform Abstract: The Quinoline Route to Pyrrolo[4,3,2-de]quinoline-Containing Marine Natural Products
  82. Ellipticine, uleine, apparicine, and related alkaloids
  83. Synthesis of deoxyvariolin B
  84. Cyclic ureas as ortho directing substituents
  85. ChemInform Abstract: Preparation of New Pyridoacridine Derivatives and Formal Synthesis of 11-Hydroxyascididemine.
  86. Preparation of New Pyridoacridine Derivatives and Formal Synthesis of 11-Hydroxyascididemine
  87. Synthesis of Ascididemine and an Isomer
  88. 1H NMR spectroscopy with internal and external standards for the quantification of libraries
  89. Syntheses of Batzelline A, Batzeline B, Isobatzelline A, and Isobatzelline B
  90. Synthesis of 3-Aryl- and 3-Heteroaryl-7-azaindoles
  91. Synthesis of 1,2-dihydropyrrolo[1,2-c]pyrimidin-1-ones
  92. Synthesis of two pyranoquinolinones. What is the structure of cherimoline ?
  93. Synthesis of isobatzelline B
  94. Conversion of a 4-quinolone into a 1,6-diazaphenalene
  95. Synthesis of pyrido[2,3-b]acridine-5,11,12-triones
  96. Synthesis of Methyl 2-Acetylamino-5-(1,3-dithian-2-yl)thiazole-4-carboxylate
  97. Synthesis of 6-chloro-1,3,4,5-tetrahydro-7,8-dimethoxy-1-methylpyrrolo[4,3,2-de]quinoline from a quinoline; Formal total syntheses of batzelline C, isobatzelline C, discorhabdin C and makaluvamine D
  98. Nucleophilic Substitution of 7-Chloro-1-Methyl-4-Quinolone
  99. Synthesis of damirones A and B from a quinoline
  100. Synthesis of Some Pyrrolo[4,3,2-de]quinolines
  101. Synthesis of benz[b]acridine-6,11,12-triones
  102. Synthesis of a 1,3,4,5-Tetrahydropyrrolo[4,3,2-de]quinoline
  103. Synthesis of a 1,3,4,5-tetrahydropyrrolo[4,3,2-de]quinoline from a Quinoline
  104. An improved annelation method with methyl2-(1,3-dithian-2-yl)benzoate as a bidentate synthon
  105. Hetero-ring lithiation of N-methyl-4-quinolone and N-methylquinoline-4-thione
  106. Reactions of 1-methyl-4-quinolone with 2-lithio-1,3-dithianes
  107. Synthesis of Pyridoacridines
  108. Studies on the synthesis of indole alkaloids
  109. Marine, Nitrogen-containing Heterocyclic Natural Products — Structures and Syntheses of Compounds Containing Indole Units
  110. Marine, Nitrogen-containing Heterocyclic Natural Products. Structures and Syntheses of Compounds Containing Quinoline and/or Isoqiunoline Units
  111. Dimethyl(methylthio)sulfonium fluoroborate induced cyclization of dithioacetals upon 2,3-disubstituted indoles
  112. Addition of Indoles to N-Alkylpyridinium Salts. Synthesis of (Dihydropyridyl)indoles
  113. A new strategy for the synthesis of pentacyclic Strychnos alkaloids: synthesis of (±)-tubifolidine
  114. Addition of Stabilized Carbon Nucleophiles to N-Alkylpyridinium Salts. Applications to Alkaloids Synthesis
  115. Studies on the synthesis of strychnos indole alkaloids
  116. Studies on the synthesis of indole alkaloids. A direct entry to 4-ethylidene-hexahydro-1,5-methanoazocino[4,3-]indoles
  117. A proton magnetic resonance study of isomeric alkylidencyanoesters
  118. The title describes a protecting group of amines for its use in solid phase peptide synthesis