Application of oxonolysis to the study of substituted derivatives of vulpinic acid: constitution of pinastric and isopinastric acids

Agarwal, S. C. ; Seshadri, T. R. (1963) Application of oxonolysis to the study of substituted derivatives of vulpinic acid: constitution of pinastric and isopinastric acids Tetrahedron, 19 (12). pp. 1965-1968. ISSN 0040-4020

Full text not available from this repository.

Official URL: http://www.sciencedirect.com/science/article/pii/0...

Related URL: http://dx.doi.org/10.1016/0040-4020(63)85010-3

Abstract

Oxonolysis of vulpinic acid (V) yields the methyl ester of benzoylformic acid as the neutral product indicating the possibility of identifying the ester half of the molecule. In this reaction pinastric acid and isopinastric acid gave methyl benzoylformate and methyl p-methoxybenxoylformate respectively and these results confirm the revised structures I and II assigned to them as position isomers.

Item Type:Article
Source:Copyright of this article belongs to Elsevier Science.
ID Code:68124
Deposited On:02 Nov 2011 11:18
Last Modified:02 Nov 2011 11:18

Repository Staff Only: item control page