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
- 1 October 1997
- journal article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 119 (41) , 9915-9916
- https://doi.org/10.1021/ja9713690
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- Peptide Synthesis via Amino Acid HalidesAccounts of Chemical Research, 1996
- Efficiency in Peptide Coupling: 1-Hydroxy-7-azabenzotriazole vs 3,4-Dihydro-3-hydroxy-4-oxo-1,2,3-benzotriazineThe Journal of Organic Chemistry, 1995
- Advantageous applications of azabenzotriazole (triazolopyridine)-based coupling reagents to solid-phase peptide synthesisJournal of the Chemical Society, Chemical Communications, 1994
- The 2-chloro-3-indenylmethyloxycarbonyl and benz[f]inden-3-ylmethyloxycarbonyl base-sensitive amino-protecting group. Application to an inverse Merrifield approach to peptide synthesisThe Journal of Organic Chemistry, 1990
- Preparation of oligomer‐free Nα‐Fmoc and Nα‐urethane amino acidsInternational Journal of Peptide and Protein Research, 1989
- The ((.beta.-phenylethyl)oxy)carbonyl ("homobenzyloxycarbonyl", hZ) amino-protecting groupThe Journal of Organic Chemistry, 1986
- Introduction of 9-fluorenylmethyloxycarbonyl, trichloroethoxycarbonyl, and benzyloxycarbonyl amine protecting groups into O-unprotected hydroxyamino acids using succinimidyl carbonatesCanadian Journal of Chemistry, 1982
- Reagents for the crosslinking of proteins by equilibrium transfer alkylationJournal of the American Chemical Society, 1979
- Side reactions in peptide synthesis. 11. Possible removal of the 9-fluorenylmethyloxycarbonyl group by the amino components during couplingThe Journal of Organic Chemistry, 1979