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A regiospecific route to conjugated enones viaα-phenylthio ketones

Authors :
John Durman
Andrew B. McElroy
Jason Elliott
Stuart Warren
Source :
J. Chem. Soc., Perkin Trans. 1. :1237-1244
Publication Year :
1985
Publisher :
Royal Society of Chemistry (RSC), 1985.

Abstract

2,5-Dimethylhex-4-en-3-one, E-6-methylhept-2-en-4-one, E-7-methyloct-4-en-3-one, ar-turmerone, and E-7-oxo-act-5-enoic acid were synthesized regiospecifically viaα-phenylthio ketones from bisphenylthio carbanions and aldehydes.

Details

ISSN :
13645463 and 0300922X
Database :
OpenAIRE
Journal :
J. Chem. Soc., Perkin Trans. 1
Accession number :
edsair.doi...........4a2c5ee8ead76cf43b2d847eac2d9fbb