Catalytic asymmetric synthesis of polysubstituted spirocyclopropyl oxindoles: Organocatalysis versus transition metal catalysis

Zhong Yan Cao, Jian Zhou

Research output: Contribution to journalReview articlepeer-review

118 Scopus citations

Abstract

Spirocyclopropyl oxindoles are widely present in natural products and bioactive molecules. In addition, they play a significant role as a type of donor-acceptor (DA) cyclopropanes in catalytic reactions. Four distinct pathways have been developed for the asymmetric synthesis of this framework, which nicely show the potential of organocatalytic and metal catalyzed asymmetric cyclopropanation in the creation of spirocyclic compounds. This minireview summarizes these complementary methods to synthesise optically active spirocyclopropyl oxindoles bearing various functional groups, discusses the difference and advantages of each method, and summarizes synthetic opportunities that still exist.

Original languageEnglish
Pages (from-to)849-858
Number of pages10
JournalOrganic Chemistry Frontiers
Volume2
Issue number7
DOIs
StatePublished - Jul 2015

Fingerprint

Dive into the research topics of 'Catalytic asymmetric synthesis of polysubstituted spirocyclopropyl oxindoles: Organocatalysis versus transition metal catalysis'. Together they form a unique fingerprint.

Cite this