Issue 8, 1970

Cope rearrangement of some germacrane-type furan sesquiterpenes. Part I

Abstract

Cope rearrangements of some germacrane-type furan sesquiterpenes have been examined and the absolute configuration of the rearrangement products has been confirmed. The results suggest that the stereochemistry of the rearrangement product is controlled by the conformation of the ten-membered ring compound.

Article information

Article type
Paper

J. Chem. Soc. C, 1970, 1142-1147

Cope rearrangement of some germacrane-type furan sesquiterpenes. Part I

K. Takeda, I. Horibe and H. Minato, J. Chem. Soc. C, 1970, 1142 DOI: 10.1039/J39700001142

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