Asymmetric synthesis of druglike six-membered spirooxindoles through an amino enyne catalysis

D. B. Ramachary*, Chintalapudi Venkaiah, R. Madhavachary

*Corresponding author for this work

Research output: Contribution to journalArticle (Academic Journal)peer-review

73 Citations (Scopus)

Abstract

An effective reflexive-Michael (r-M) reaction has been disclosed to access drug-like six-membered spirooxindoles in good yields and excellent enantioselectivities by using an aminoenyne-catalysis.

Original languageEnglish
Pages (from-to)3042-3045
Number of pages4
JournalOrganic Letters
Volume15
Issue number12
DOIs
Publication statusPublished - 21 Jun 2013

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