Tetrahedron Letters p. 169 - 172 (1992)
Update date:2022-09-26
Topics:
Hoye, Thomas R.
Dinsmore, Christopher J.
Acetylenic α-diazaketones 1, when treated with catalytic rhodium carboxylate dimer and diallylsulfide (1.1 equiv), undergo sequential alkyne insertion/ylide formation/sigmatropic rearrangements to give γ-allylthio cyclic enones.This transformation was use
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(2019)Doi:10.1016/S0040-4039(00)92332-3
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