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Organocatalytic Kinetic Resolution Cascade Reactions: New Mechanistic and Stereochemical Manifold in Diphenyl Prolinol Silyl Ether Catalysis
Author(s) -
McGarraugh Patrick G.,
Johnston Ryne C.,
MartínezMuñoz Aurora,
Cheong Paul HaYeon,
BrennerMoyer Stacey E.
Publication year - 2012
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201104029
Subject(s) - iminium , chemistry , enamine , cascade reaction , kinetic resolution , catalysis , silylation , intramolecular force , asymmetric induction , intermolecular force , organocatalysis , silyl ether , combinatorial chemistry , enantioselective synthesis , organic chemistry , molecule
A new cascade reaction involving an iminium‐catalyzed intramolecular oxa‐Michael addition followed by an enamine‐catalyzed intermolecular Michael addition is reported herein. This cascade reaction generates enantiopure, highly functionalized tetrahydropyrans and tetrahydrofurans in a one‐pot reaction and in up to 89 % combined yield and up to 99 % ee . This cascade reaction is catalyzed by diaryl prolinol silyl ethers, which are a privileged class of catalysts. The stereochemical outcome of these cascade reactions is unprecedented. Computational studies indicate that this stereochemical outcome arises from nonclassical hydrogen‐bonding interactions between the electrophile and the substrate, and from entropic considerations of preorganization. The unprecedented configurations of the cascade products, combined with the computational models, reveal for the first time that asymmetric induction by diaryl prolinol silyl ether catalysts is not always exclusively reagent controlled. The stereochemical outcome also arises from a kinetic resolution or dynamic kinetic resolution of the β‐stereocenter through an enamine‐catalyzed intermolecular reaction. This unprecedented organocascade reaction mechanism may be adaptable to diaryl prolinol silyl ether‐catalyzed cascade reactions, in which both the iminium‐ and enamine‐catalyzed steps are intermolecular, an underdeveloped type of cascade reaction.