88065-33-2Relevant academic research and scientific papers
A Regiospecific Route to Conjugated Enones via α-Phenylthio Ketones
Durman, John,Elliott, Jason,McElroy, Andrew B.,Warren, Stuart
, p. 1237 - 1244 (2007/10/02)
2,5-Dimethylhex-4-en-3-one, E-6-methylhept-2-en-4-one, E-7-methyloct-4-en-3-one, ar-tumerone, and E-7-oxo-oct-5-enoic acid were synthesized regiospecifically via α-phenylthio ketones from bisphenylthio carbanions and aldehydes.
REGIOSPECIFIC SYNTHESIS OF ENONES VIA α-(PHENYLTHIO)-KETONES: 2,5-DIMETHYL-4-HEXEN-3-ONE, E-6-METHYL-2-HEPTEN-4-ONE, E-7-METHYL-4-OCTEN-3-ONE, AND AR-TURMERONE
Durman, John,Elliott, Jason,McElroy, Andrew B.,Warren, Stuart
, p. 3927 - 3930 (2007/10/02)
Enones not available from aldol condensations may be synthesised regiospecifically via α-(phenylthio)ketones: the title compounds have been made by this route.
