Asymmetric synthesis of druglike six-membered spirooxindoles through an amino enyne catalysis
Asymmetric synthesis of druglike six-membered spirooxindoles through an amino enyne catalysis
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Date
2013-06-21
Authors
Ramachary, D. B.
Venkaiah, Chintalapudi
Madhavachary, R.
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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. © 2013 American Chemical Society.
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Organic Letters. v.15(12)