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- W1974443997 endingPage "1407" @default.
- W1974443997 startingPage "1381" @default.
- W1974443997 abstract "Abstract The 3,3′‐disubstituted oxindole structural motif is a prominent feature in many alkaloid natural products, which include all kinds of tetrasubstituted carbon stereocenters, spirocyclic or not, all‐carbon or heteroatom‐containing. The catalytic asymmetric synthesis of the tetrasubstituted carbon stereocenter at the C‐3 position of the oxindole framework integrates new synthetic methods and chiral catalysts, reflects the latest achievements in asymmetric catalysis, and facilitates the synthesis of sufficient quantities of related compounds as potential medicinal agents and biological probes. This review summarizes the recent progress in this area, and applications in the total synthesis of related bioactive compounds." @default.
- W1974443997 created "2016-06-24" @default.
- W1974443997 creator A5032643990 @default.
- W1974443997 creator A5032911060 @default.
- W1974443997 creator A5045245504 @default.
- W1974443997 date "2010-06-01" @default.
- W1974443997 modified "2023-10-18" @default.
- W1974443997 title "Catalytic Asymmetric Synthesis of Oxindoles Bearing a Tetrasubstituted Stereocenter at the C-3 Position" @default.
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