Asymmetric Synthesis of Druglike Six-Membered Spirooxindoles through an Amino Enyne Catalysis

Ramachary, D. B. ; Venkaiah, Chintalapudi ; Madhavachary, R. (2013) Asymmetric Synthesis of Druglike Six-Membered Spirooxindoles through an Amino Enyne Catalysis Organic Letters, 15 (12). pp. 3042-3045. ISSN 1523-7060

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Official URL: http://doi.org/10.1021/ol401227q

Related URL: http://dx.doi.org/10.1021/ol401227q

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.

Item Type:Article
Source:Copyright of this article belongs to American Chemical Society.
ID Code:120674
Deposited On:03 Jul 2021 07:55
Last Modified:03 Jul 2021 07:55

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