Development of Biligands Magnesium Catalysis in Asymmetric Conjugate Reactions of C3-Pyrrolyl-Oxindoles
Oxindole
Conjugate
DOI:
10.1021/acs.orglett.7b02044
Publication Date:
2017-07-28T12:49:13Z
AUTHORS (9)
ABSTRACT
A magnesium catalyzed asymmetric conjugate reaction of C3-pyrrolyl-oxindoles with terminal alkynones is presented. The current relies on the development novel combinational catalysis involving two chiral ligands. protocol proceeds smoothly and gives corresponding enantioenriched 3,3-disubstituted oxindole skeletons good enantioselectivities. Furthermore, adducts could be transferred to spiro structures containing an eight-membered ring in high ee values.
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