ACETYL CHLORIDE-METHANOL AS A CONVENIENT REAGENT FOR - A) QUANTITATIVE FORMATION OF AMINE HYDROCHLORIDES B) CARBOXYLATE ESTER FORMATION C) MILD REMOVAL OF N-T-BOC-PROTECTIVE GROUP

Authors
NUDELMAN A BECHOR Y FALB E FISCHER B WEXLER BA NUDELMAN A
Citation
A. Nudelman et al., ACETYL CHLORIDE-METHANOL AS A CONVENIENT REAGENT FOR - A) QUANTITATIVE FORMATION OF AMINE HYDROCHLORIDES B) CARBOXYLATE ESTER FORMATION C) MILD REMOVAL OF N-T-BOC-PROTECTIVE GROUP, Synthetic communications, 28(3), 1998, pp. 471-474
Citations number
3
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Synthetic communications → ACNP
ISSN journal
00397911
Volume
28
Issue
3
Year of publication
1998
Pages
471 - 474
Database
ISI
SICI code
0039-7911(1998)28:3<471:ACAACR>2.0.ZU;2-E
Abstract
Hydrogen chloride quatitativaly generated in situ by the addition of a cetyl chloride to alcoholic solutions is a useful reagent for carboxyl ic acid esterification, N-t-Boc deprotection and phosphoramide solvoly sis reactions.