Chemistry Letters p. 1159 - 1160 (1981)
Update date:2022-09-26
Topics:
Fujisawa, Tamotsu
Noda, Atsunari
Kawara, Tatsuo
Sato, Toshio
Trapping of an enolate anion, formed by the Michael addition, with methanesulfinyl chloride and subsequent desulfinylation is found to be a useful method for the synthesis of various α,β-unsaturated carbonyl compounds.Synthetic utility of this method is demonstrated in the synthesis of geraniol, nerol, farnesol, and dihydrojasmone.
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Doi:10.1016/S0040-4020(01)97990-6
(1981)Doi:10.1016/S0040-4020(01)88649-X
(1983)Doi:10.1055/s-2004-831163
(2004)Doi:10.1248/cpb.29.2691
(1981)Doi:10.1039/P19810002764
(1981)Doi:10.1246/bcsj.54.3088
(1981)
