Boc-L-Dmt-OH as a fully N,S-blocked cysteine derivative for peptide synthesis by prior thiol capture. Facile conversion of N-terminal Boc-L-Dmt-peptides to H-Cys(Scm)-peptides
- 1 July 1989
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 54 (15) , 3640-3646
- https://doi.org/10.1021/jo00276a026
Abstract
No abstract availableKeywords
This publication has 4 references indexed in Scilit:
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- Rational design of templates for intramolecular O,N-acyl transfer via medium-sized cyclic intermediates derived from L-cysteine. Definition of an experimental maximum in effective molarity through the study of "tunable" templatesThe Journal of Organic Chemistry, 1989
- Solid‐phase peptide synthesis: a silver anniversary report*International Journal of Peptide and Protein Research, 1987
- Peptide synthesis by prior thiol capture. 1. A convenient synthesis of 4-hydroxy-6-mercaptodibenzofuran and novel solid-phase synthesis of peptide-derived 4-(acyloxy)-6-mercaptodibenzofuransThe Journal of Organic Chemistry, 1986