Jump to main content
Jump to site search
PLANNED MAINTENANCE Close the message box

Scheduled maintenance work on Wednesday 21st October 2020 from 07:00 AM to 07:00 PM (BST).

During this time our website performance may be temporarily affected. We apologise for any inconvenience this might cause and thank you for your patience.

Issue 5, 2001
Previous Article Next Article

Photocycloaddition reactions of 2-acylcyclohex-2-enones

Author affiliations


The newly synthesized 2-acylcyclohex-2-enones 1 photocycloadd selectively to the C–C triple bond of 2-methylbut-1-en-3-yne giving diacylcyclobutene derivatives 4 and 5, and they react with 2,3-dimethylbut-2-ene in an overall [4+2]-photocycloaddition to afford benzopyranones 7.

Back to tab navigation

Article information

28 Nov 2000
06 Feb 2001
First published
19 Feb 2001

Chem. Commun., 2001, 481-482
Article type

Photocycloaddition reactions of 2-acylcyclohex-2-enones

L. O. Ferrer and P. Margaretha, Chem. Commun., 2001, 481
DOI: 10.1039/B009692J

Social activity

Search articles by author