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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Doi:10.1021/acs.inorgchem.9b00072
(2019)Doi:10.1016/S0040-4039(00)92332-3
(1992)Doi:10.1080/00397911.2014.947652
(2014)Doi:10.1016/j.ijpharm.2012.08.023
(2012)Doi:10.1021/acs.orglett.6b02599
(2016)Doi:10.1021/ol302751b
(2012)
