Issue 20, 1969

Photorearrangement of a γ-butyrolactone: generation of intermediates in photochemical reactions

Abstract

The photolysis of 6,7,8,9-tetrahydro-9-hydroxy-7-oxo-5,8-methano-5H-benzocycloheptene-10-carboxylic acid lactone yields, in addition to CO2, naphthalene, keten, 3,4-benzotricyclo[3,3,0,02,8]octan-7-one, and benzobicyclo[2,2,2]octadienone, the same products obtained from the sensitized photolysis of benzobicyclo[2,2,2]octadienone.

Article information

Article type
Paper

J. Chem. Soc. D, 1969, 1164-1165

Photorearrangement of a γ-butyrolactone: generation of intermediates in photochemical reactions

R. S. Givens and W. F. Oettle, J. Chem. Soc. D, 1969, 1164 DOI: 10.1039/C29690001164

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements