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

dc.contributor.author Ramachary, D. B.
dc.contributor.author Venkaiah, Chintalapudi
dc.contributor.author Madhavachary, R.
dc.date.accessioned 2022-03-27T09:39:56Z
dc.date.available 2022-03-27T09:39:56Z
dc.date.issued 2013-06-21
dc.description.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.
dc.identifier.citation Organic Letters. v.15(12)
dc.identifier.issn 15237060
dc.identifier.uri 10.1021/ol401227q
dc.identifier.uri https://pubs.acs.org/doi/10.1021/ol401227q
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/13173
dc.title Asymmetric synthesis of druglike six-membered spirooxindoles through an amino enyne catalysis
dc.type Journal. Article
dspace.entity.type
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