A Stereospecific Synthesis of Trisubstituted Alkenes via Hydridation of Dialkylhaloboranes Followed by Hydroboration-Iodination of Internal Alkynes

dc.contributor.author Brown, Herbert C.
dc.contributor.author Basavaiah, D.
dc.contributor.author Kulkarni, Surendra U.
dc.date.accessioned 2022-03-27T09:06:13Z
dc.date.available 2022-03-27T09:06:13Z
dc.date.issued 1982-01-01
dc.description.abstract Dialkylvinylboranes, prepared conveniently via the hydridation of dialkylhaloboranes in the presence of an internal alkyne, react with iodine under basic conditions to produce trisubstituted alkenes of established stereochemistry, providing a general synthesis of trisubstituted alkenes with unambiguous stereochemistry. © 1982, American Chemical Society. All rights reserved.
dc.identifier.citation Journal of Organic Chemistry. v.47(1)
dc.identifier.issn 00223263
dc.identifier.uri 10.1021/jo00340a045
dc.identifier.uri https://pubs.acs.org/doi/abs/10.1021/jo00340a045
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/12419
dc.title A Stereospecific Synthesis of Trisubstituted Alkenes via Hydridation of Dialkylhaloboranes Followed by Hydroboration-Iodination of Internal Alkynes
dc.type Journal. Letter
dspace.entity.type
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