Acetyl bromide-alcohols as convenient reaction systems for: a) removal of N-tert-Boc, N-CBZ and N-Ac protective groups b) esterifications and transesterification c) debenzylation of aryl-O-benzyl ethers

Authors
Lesk, A Nudelman, A
Citation
A. Lesk et A. Nudelman, Acetyl bromide-alcohols as convenient reaction systems for: a) removal of N-tert-Boc, N-CBZ and N-Ac protective groups b) esterifications and transesterification c) debenzylation of aryl-O-benzyl ethers, SYN COMMUN, 29(8), 1999, pp. 1405-1408
Citations number
2
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
SYNTHETIC COMMUNICATIONS
ISSN journal
00397911 → ACNP
Volume
29
Issue
8
Year of publication
1999
Pages
1405 - 1408
Database
ISI
SICI code
0039-7911(1999)29:8<1405:ABACRS>2.0.ZU;2-R
Abstract
Hydrogen bromide generated in situ by the addition of acetyl bromide to alc ohols is a useful reagent for esterifications and transesterifications; N-t ert-Boc, N-Cbz and N-Ac deprotections; and debenzylation reactions.