DURMAN, J.;ELLIOTT, J.;MCELROY, A. B.;WARREN, S., J. CHEM. SOC. PERKIN TRANS., 1985, N 6, 1237-1244
作者:DURMAN, J.、ELLIOTT, J.、MCELROY, A. B.、WARREN, S.
DOI:——
日期:——
A regiospecific route to conjugated enones viaα-phenylthio ketones
作者:John Durman、Jason Elliott、Andrew B. McElroy、Stuart Warren
DOI:10.1039/p19850001237
日期:——
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.
Regiospecific synthesis of enones α-(phenylthio)-ketones: 2,5-dimethyl-4-hexen-3-one, -6-methyl-2-hepten-4-one, -7-methyl-4-octen-3-one, and ar-turmerone
作者:John Durman、Jason Elliott、Andrew B. McElroy、Stuart Warren
DOI:10.1016/s0040-4039(00)94317-x
日期:1983.1
Enones not available from aldol condensations may be synthesised regio-specifically α-(phenylthio)ketones: the title compounds have been made by this route.