Issue 19, 1971

The mechanism of the photochemical cyclisation of non-conjugated dienes: dimethyl nona-2,7-diene-1,9-dioate

Abstract

Photolysis of acetone solutions of the cis,cis-, the cis,trans-, and the trans,trans-1,6-dienes (VIa–c) leads in each case to cis–trans-isomerization and, at a comparable rate, to formation of the cyclised products (VII) and (VIII).

Article information

Article type
Paper

J. Chem. Soc. D, 1971, 1217-1218

The mechanism of the photochemical cyclisation of non-conjugated dienes: dimethyl nona-2,7-diene-1,9-dioate

J. R. Scheffer, R. A. Wostradowski and K. C. Dooley, J. Chem. Soc. D, 1971, 1217 DOI: 10.1039/C29710001217

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