Synthesis p. 1088 - 1091 (1987)
Update date:2022-08-03
Topics:
Marino, Joseph P.
Pradilla, Roberto Fernandez de la
Laborde, Edgardo
The application of a chiral sulfoxide-directed lactonization to the synthesis of a precursor of the neolignan porosin, in optically active form, is described.The methodology provides an efficient access to 3,4-disubstituted γ-butyrolactones with complete
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Doi:10.1002/ejoc.201300505
(2013)Doi:10.1021/jo00255a038
(1988)Doi:10.1021/jo00256a004
(1988)Doi:10.1016/S0040-4020(01)83447-5
(1987)Doi:10.1246/cl.1988.91
(1988)Doi:10.1039/b901173k
(2009)
