164 results on '"Carpino, Louis A."'
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2. N,O-Acyl Shifts: Unexpected Side-Reaction and Beneficial Tool in Fmoc-Chemistry
3. Synthesis of the Two Isomeric Benzo Derivatives of 1-Hydroxy-7-azabenzotriazole and Preliminary Studies of Their Effectiveness as Coupling Reagents
4. [7] Coupling reagents and activation
5. On the use of novel coupling reagents for solid-phase peptide synthesis
6. Solid phase peptide synthesis using Fmoc amino acid fluorides
7. Use of Fmoc amino acid chlorides in peptide synthesis
8. Protected amino acid chlorides: Coupling reagents suitable for the most highly hindered systems
9. t ‐Butyl carbazate
10. ChemInform Abstract: The 1,1-Dioxobenzo[b]thiophene-2-ylmethyloxycarbonyl (Bsmoc) Amino-Protecting Group.
11. ChemInform Abstract: Amino-Protecting Groups Subject to Deblocking under Conditions of Nucleophilic Addition to a Michael Acceptor. Structure-Reactivity Studies and Use of the 2-(tert-Butylsulfonyl)-2-propenyloxycarbonyl (Bspoc) Group.
12. ChemInform Abstract: The 2-Methylsulfonyl-3-phenyl-1-prop-2-enyloxycarbonyl (Mspoc)Amino-Protecting Group.
13. ChemInform Abstract: The Solid State and Solution Structure of HAPyU (I).
14. On the use of N -dicyclopropylmethyl aspartyl-glycine synthone for backbone amide protection
15. Dicyclopropylmethyl Peptide Backbone Protectant†
16. Segment coupling to a highly hindered N-terminal, alamethicin-related α-aminoisobutyric acid (Aib) residue
17. 1,1-Dioxonaphtho[1,2-b]thiophene-2-methyloxycarbonyl (α-Nsmoc) and 3,3-Dioxonaphtho[2,1-b]thiophene-2-methyloxycarbonyl (β-Nsmoc) Amino-Protecting Groups
18. Depsipeptide Methodology for Solid-Phase Peptide Synthesis: Circumventing Side Reactions and Development of an Automated Technique via Depsidipeptide Units,
19. Dramatically enhanced N→O acyl migration during the trifluoroacetic acid-based deprotection step in solid phase peptide synthesis
20. Synthesis of ‘difficult’ peptide sequences: application of a depsipeptide technique to the Jung–Redemann 10- and 26-mers and the amyloid peptide Aβ(1–42)
21. Organophosphorus and Nitro-Substituted Sulfonate Esters of 1-Hydroxy-7-azabenzotriazole as Highly Efficient Fast-Acting Peptide Coupling Reagents.
22. Organophosphorus and Nitro-Substituted Sulfonate Esters of 1-Hydroxy-7-azabenzotriazole as Highly Efficient Fast-Acting Peptide Coupling Reagents
23. 3-Hydroxy-4-oxo-3,4-dihydro-5-azabenzo-1,2,3-triazene
24. Synthesis of the Two Isomeric Benzo Derivatives of 1-Hydroxy-7-azabenzotriazole and Preliminary Studies of Their Effectiveness as Coupling Reagents
25. 2,3-Diphenylvinylene Sulfone
26. t ‐Butyl azodiformate
27. t-Butyl azidoformate
28. α,α′-Dibromodibenzyl Sulfone
29. α,α-Dimethyl Cyclopropanemethanamine
30. Complex Polyfluoride Additives in Fmoc-Amino Acid Fluoride Coupling Processes. Enhanced Reactivity and Avoidance of Stereomutation†
31. Rapid, Continuous Solution-Phase Peptide Synthesis: Application to Peptides of Pharmaceutical Interest
32. α-Cyclopropylcyclopropanemethanol
33. 1,1-Dioxobenzo[b]-thiophene-2-yl Methyloxycarbonyl Chloride
34. Kupplungsreagentien vom Uronium-/Guanidinium-Typ: Synthese und Charakterisierung der authentischen Uroniumsalze
35. Kupplungsreagentien vom Uronium-/Guanidinium-Typ: Synthese und Charakterisierung der authentischen Uroniumsalze
36. The Uronium/Guanidinium Peptide Coupling Reagents: Finally the True Uronium Salts
37. The 5,6- and 4,5-Benzo Derivatives of 1-Hydroxy-7-azabenzotriazole
38. The Solid State and Solution Structure of HAPyU,,
39. N-[(Dimethylamino)-1H-1,2,3-triazolo[4,5-b]pyridin-1-ylmethylene]-N-methylmethanaminium HexafluorophosphateN-Oxide
40. 3-Hydroxy-3H-1,2,3-triazolo[4,5-b]pyridine
41. Solubilizing Influence of 2,7-Bis(trimethylsilyl) Substitution on the Fmoc Residue
42. Substituted Guanidines: Introducing Diversity in Combinatorial Chemistry
43. Comparison of the Effects of 5- and 6-HOAt on Model Peptide Coupling Reactions Relative to the Cases for the 4- and 7-Isomers,
44. The 2-Methylsulfonyl-3-phenyl-1-prop-2- enyloxycarbonyl (Mspoc)Amino-Protecting Group
45. Amino-Protecting Groups Subject to Deblocking under Conditions of Nucleophilic Addition to a Michael Acceptor. Structure−Reactivity Studies and Use of the 2-(tert-Butylsulfonyl)-2-propenyloxycarbonyl (Bspoc) Group
46. The 1,1-Dioxobenzo[b]thiophene-2-ylmethyloxycarbonyl (Bsmoc) Amino-Protecting Group
47. The diisopropylcarbodiimide/ 1-hydroxy-7-azabenzotriazole system: Segment coupling and stepwise peptide assembly
48. 2-Propanephosphonic acid anhydride (T3P)-mediated segment coupling and head-to-tail cyclization of sterically hindered peptides
49. Protected amino acid chlorides vs protected amino acid fluorides: Reactivity comparisons
50. New Family of Base- and Nucleophile-Sensitive Amino-Protecting Groups. A Michael-Acceptor-Based Deblocking Process. Practical Utilization of the 1,1-Dioxobenzo[b]thiophene-2-ylmethyloxycarbonyl (Bsmoc) Group
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