Studies on peptides. CLII. Hard acid deprotecting procedure for peptide synthesis.
- 1 January 1987
- journal article
- research article
- Published by Pharmaceutical Society of Japan in CHEMICAL & PHARMACEUTICAL BULLETIN
- Vol. 35 (8), 3447-3452
- https://doi.org/10.1248/cpb.35.3447
Abstract
The use of trimethylsilyl triflujoromethanesulfonate as a peptide deprotecting reagent was examined, together with the role of soft bases employed. A new deprotecting procedure based on the hard acid principle is presented.This publication has 2 references indexed in Scilit:
- Mechanisms for the removal of benzyl protecting groups in synthetic peptides by trifluoromethanesulfonic acid-trifluoroacetic acid-dimethyl sulfideJournal of the American Chemical Society, 1986
- Studies on peptides. CXXI. Nin-Mesitylenesulfonyltryptophan, a new derivative for peptide synthesis.CHEMICAL & PHARMACEUTICAL BULLETIN, 1984