Photoannelations with α-Formyl Ketones. Enol Specificity in the Reaction of Acyclic α-Formyl Ketones with Alkenes
Journal Article (Letter;Journal)
The irradiation of several acyclic α-formyl ketones in the presence of alkenes gives rise to photoproducts derived exclusively from that tautomer enolized toward the aldehyde carbonyl, which can then be cyclized to provide a new cyclohexenone annelation sequence. © 1975, American Chemical Society. All rights reserved.
Full Text
Duke Authors
Cited Authors
- Baldwin, SW; Gawley, RE; Doll, RJ; Leung, KH
Published Date
- June 1, 1975
Published In
Volume / Issue
- 40 / 12
Start / End Page
- 1865 - 1867
Electronic International Standard Serial Number (EISSN)
- 1520-6904
International Standard Serial Number (ISSN)
- 0022-3263
Digital Object Identifier (DOI)
- 10.1021/jo00900a052
Citation Source
- Scopus