Author:
Chu Daniel T. W.,Bernstein Edith,Huckin Stuart N.
Abstract
The properties of the 1,3-cyclohexanedione system in 2-deacetylchelocardin (2) and N-carbobenzoxy-2-deacetylchelocardin (3) are found to be significantly different from those of ordinary 1,3-cyclohexanediones. Acylation and alkylation of (2) or (3) generally gives O-acylation or O-alkylation products. However, reaction of N-carbobenzoxy-2-deacetylchelocardin (3) with methyl orthoformate or N,N-dimethylformamide dimethyl acetal leads exclusively to C-acylation products.
Publisher
Canadian Science Publishing
Subject
Organic Chemistry,General Chemistry,Catalysis
Cited by
3 articles.
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