STUDIES IN RING EXPANSION,
Abstract
In contrast to an enolizable dimedone derivative, the non-enolizable 2-methyl-2-(2'-benzoyl ethyl)-dimedone was cyclised to 1-methyl-4-phenyl bicyclo(3,3,1)non-3-en -8.9-dione. The infrared spectrum of this and other non-enolizable beta-diketones shows a split carbonyl band. This phenomenon was investigated. A new cycloheptene synthesis previously reported was applied to the synthesis of a compound related to the alkaloid colchicine. (Author)
Document Details
- Document Type
- Technical Report
- Publication Date
- Dec 31, 1964
- Accession Number
- AD0628733
Entities
People
- G. L. Buchanan
Organizations
- University of Glasgow