Stereoselective synthesis of five-membered spirooxindoles through Tomita zipper cyclization

dc.contributor.author Ramachary, D. B.
dc.contributor.author Venkaiah, Chintalapudi
dc.contributor.author Krishna, Patoju M.
dc.date.accessioned 2022-03-27T09:39:50Z
dc.date.available 2022-03-27T09:39:50Z
dc.date.issued 2013-09-20
dc.description.abstract Functionalized five-membered spirooxindoles were furnished in good yields and excellent stereoselectivities by using an effective Tomita zipper cyclization (TZC) reaction through organophosphine catalysis. © 2013 American Chemical Society.
dc.identifier.citation Organic Letters. v.15(18)
dc.identifier.issn 15237060
dc.identifier.uri 10.1021/ol4020305
dc.identifier.uri https://pubs.acs.org/doi/10.1021/ol4020305
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/13171
dc.title Stereoselective synthesis of five-membered spirooxindoles through Tomita zipper cyclization
dc.type Journal. Article
dspace.entity.type
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