All Stories

  1. Synthesis, Characterization of Novel Morpholino-1, 3, 5-Triazinyl Amino Acid Ester Derivatives and their Anti-Proliferation Activities
  2. Production and physicochemical assessment of new stevia amino acid sweeteners from the natural stevioside
  3. Methods for the Peptide Synthesis and Analysis
  4. Peptide synthesis beyond DMF: THF and ACN as excellent and friendlier alternatives
  5. TOMBU and COMBU as Novel Uronium-Type Peptide Coupling Reagents Derived from Oxyma-B
  6. ChemInform Abstract: Advances in Acylation Methodologies Enabled by Oxyma-Based Reagents
  7. Low-epimerization Peptide Bond Formation with Oxyma Pure: Preparation of Z-L-Phg-Val-OMe
  8. Organophosphinic Coupling Reagents in Peptide Synthesis
  9. Synthesis, Characterization and Anti-proliferation Activities of Novel Cyano Oximino Sulfonate Esters
  10. OxymaPure/DIC: An Efficient Reagent for the Synthesis of a Novel Series of 4-[2-(2-Acetylaminophenyl)-2-oxo-acetylamino] Benzoyl Amino Acid Ester Derivatives
  11. K-Oxyma: a Strong Acylation-Promoting, 2-CTC Resin-Friendly Coupling Additive
  12. Synthesis, structure, theoretical calculations and biological activity of sulfonate active ester new derivatives
  13. An Efficient and Mild Method for the Synthesis and Hydrazinolysis ofN-Glyoxylamino Acid Esters
  14. Oxime-Based Carbonates as Useful Reagents for Both N-Protection and Peptide Coupling
  15. Synthesis and characterization of new polyamides derived from alanine and valine derivatives
  16. Microwave synthesis and thermal properties of polyacrylate derivatives containing itaconic anhydride moieties
  17. Microwave irradiation: A facile, scalable and convenient method for synthesis of N-phthaloylamino acids
  18. Screening ofN-Alkyl-Cyanoacetamido Oximes as Substitutes forN-Hydroxysuccinimide
  19. ChemInform Abstract: Peptide-Coupling Reagents
  20. Cyanoacetamide-based oxime carbonates: an efficient, simple alternative for the introduction of Fmoc with minimal dipeptide formation
  21. Recent development in peptide coupling reagents
  22. ChemInform Abstract: Aspartimide Formation in Peptide Chemistry: Occurrence, Prevention Strategies and the Role of N-Hydroxylamines
  23. Synthesis and Thermal Properties of Novel Polyamides Containing α-Amino Acid Moieties: Structure-Property Relationship
  24. ChemInform Abstract: Peptide Coupling Reagents - More than a Letter Soup
  25. Peptide Coupling Reagents, More than a Letter Soup
  26. Aspartimide formation in peptide chemistry: occurrence, prevention strategies and the role of N-hydroxylamines
  27. Peptide-Coupling Reagents
  28. Synthesis and Aminolysis of 2,4-Dinitrophenyl and 5-Nitropyridine N-Hydroxy Oxime Derivatives
  29. Synthesis of 2-(4,6-Dimethoxy-1,3,5-triazin-2-yloxyimino) Derivatives: Application in Solution Peptide Synthesis
  30. N-Hydroxylamines for Peptide Synthesis
  31. ChemInform Abstract: The 1,1-Dioxobenzo[b]thiophene-2-ylmethyloxycarbonyl (Bsmoc) Amino-Protecting Group.
  32. ChemInform Abstract: The Solid State and Solution Structure of HAPyU (I).
  33. A Novel Family of Onium Salts Based Upon Isonitroso Meldrum's Acid Proves Useful as Peptide Coupling Reagents
  34. PyOxP and PyOxB: the Oxyma-based novel family of phosphonium salts
  35. COMU: A third generation of uronium-type coupling reagents
  36. Microwave irradiation and COMU: a potent combination for solid-phase peptide synthesis
  37. COMU: A Safer and More Effective Replacement for Benzotriazole-Based Uronium Coupling Reagents
  38. Dicyclopropylmethyl Peptide Backbone Protectant †
  39. ChemInform Abstract: Utilization of N,N,N′,N′-Tetramethylfluoroformamidinium Hexafluorophosphate (TFFH) in Peptide and Organic Synthesis
  40. Synthesis and Application ofN-Hydroxylamine Derivatives as Potential Replacements for HOBt
  41. Utilization of N,N,N′,N′-Tetramethylfluoroformamidinium Hexafluoro­phosphate (TFFH) in Peptide and Organic Synthesis
  42. Use ofN‐Methylpiperazine for the Preparation of Piperazine‐Based Unsymmetrical Bis‐Ureas as Anti‐HIV Agents
  43. Morpholine-Based Immonium and Halogenoamidinium Salts as Coupling Reagents in Peptide Synthesis1
  44. 1,1,3,3-Tetramethylfluoroformamidinium Hexafluorophosphate
  45. Novel Proton Acceptor Immonium-Type Coupling Reagents:  Application in Solution and Solid-Phase Peptide Synthesis
  46. Reaction of Phthalaldehydic Acid with Different Substituted Aniline as well as Hydrazine Derivatives.
  47. Reaction of phthalaldehydic acid with different substituted aniline as well as hydrazine derivatives
  48. Chloroformamidinium Salts: Efficient Reagents for Preparation of 2-Aminobenzoimidazole, 2-Aminobenzoxazole, and 2-Aminobenzothiazole Derivatives.
  49. Tetramethylfluoroformamidinium hexafluorophosphate (TFFH)/benzyltriphenylphosphonium dihydrogen trifluoride (PTF): a unique reagent for the conversion of carboxylic acids to the corresponding alcohols as well as hydroxamic acids
  50. Chloroformamidinium salts: Efficient reagents for preparation of 2-aminobenzoimidazole, 2-aminobenzoxazole, and 2-aminobenzothiazole derivatives
  51. Design and Synthesis of New Immonium-Type Coupling Reagents
  52. Coupling Reactions of Hydralazine with Amino Acids and Their Adducts for Antihypertensive Activities.
  53. Coupling reactions of hydralazine with amino acids and their adducts for antihypertensive activities
  54. Organophosphorus and Nitro-Substituted Sulfonate Esters of 1-Hydroxy-7-azabenzotriazole as Highly Efficient Fast-Acting Peptide Coupling Reagents.
  55. 3-Hydroxy-4-oxo-3,4-dihydro-5-azabenzo-1,2,3-triazene†
  56. 1,1,3,3-Tetramethylfluoroformamidinium Hexafluorophosphate
  57. O-(7-Azabenzotriazol-1-yl)-1,3-dimethyl- 1,3-dimethyleneuronium Hexafluorophos-phate
  58. Complex Polyfluoride Additives in Fmoc-Amino Acid Fluoride Coupling Processes. Enhanced Reactivity and Avoidance of Stereomutation †
  59. Kupplungsreagentien vom Uronium-/Guanidinium-Typ: Synthese und Charakterisierung der authentischen Uroniumsalze
  60. A versatile synthetic route to chiral quinoxaline derivatives from amino acids precursors
  61. Substituted Guanidines:  Introducing Diversity in Combinatorial Chemistry
  62. Addition of HOXt (X = A or B) improves the efficiency of phenol-based coupling reagents during peptide synthesis
  63. The 1,1-Dioxobenzo[ b ]thiophene-2-ylmethyloxycarbonyl (Bsmoc) † Amino-Protecting Group
  64. The diisopropylcarbodiimide/ 1-hydroxy-7-azabenzotriazole system: Segment coupling and stepwise peptide assembly
  65. Use of Onium Salt-Based Coupling Reagents in Peptide Synthesis 1
  66. Bis(tetramethylene)fluoroformamidinium Hexafluorophospnate(BTFFH): A Convenient Coupling Reagent for Solid Phase Peptide Synthesis.
  67. Protected amino acid chlorides vs protected amino acid fluorides: Reactivity comparisons
  68. Spectral Characterization of Some Phenylazodihydroxy Naphthalene Derivatives
  69. Peptide Coupling in the Presence of Highly Hindered Tertiary Amines
  70. Efficiency in Peptide Coupling: 1-Hydroxy-7-azabenzotriazole vs 3,4-Dihydro-3-hydroxy-4-oxo-1,2,3-benzotriazine
  71. Tetramethylfluoroformamidinium Hexafluorophosphate: A Rapid-Acting Peptide Coupling Reagent for Solution and Solid Phase Peptide Synthesis
  72. Peptide assembly in the absence of base via Fmoc amino acid fluorides
  73. Racemization studies during solid-phase peptide synthesis using azabenzotriazole-based coupling reagents
  74. Effect of Tertiary Bases on O-Benzotriazolyluronium Salt-Induced Peptide Segment Coupling
  75. Advantageous applications of azabenzotriazole (triazolopyridine)-based coupling reagents to solid-phase peptide synthesis
  76. Bis(BOC) amino acid fluorides as reactive peptide coupling reagents
  77. Protected amino acid chlorides: Coupling reagents suitable for the most highly hindered systems