학술논문

Tributylphosphine-catalyzed acylations of alcohols: scope and related reactions
Document Type
Academic Journal
Source
Journal of Organic Chemistry. Dec 3, 1993, Vol. 58 Issue 25, p7286, 3 p.
Subject
Alcohols -- Analysis
Phosphorus compounds -- Analysis
Anhydrides -- Research
Pyridine -- Analysis
Nuclear magnetic resonance spectroscopy -- Usage
Biological sciences
Chemistry
Language
ISSN
0022-3263
Abstract
An analysis was undertaken to determine if tributylphosphine (Bu3P) is comparable to P-(dimethylamino)-pyridine (DMAP) in catalytic action. Bu3P catalysis of various electrophiles was also carried out. The counterion in the potential phosphonium intermediate and the nature of electrophilic reactant influences phosphine catalysis. DMAP catalyzes a wide range of electrophiles, making Bu3P a more flexible catalyst, as it can act as a nucleophilic catalyst and base.