A General and Stereospecific Synthesis of Cis Alkenes via Stepwise Hydroboration: A Simple Synthesis of Muscalure, the Sex Pheromone of the Housefly (Musca domestica)

dc.contributor.author Brown, Herbert C.
dc.contributor.author Basavaiah, D.
dc.date.accessioned 2022-03-27T09:06:11Z
dc.date.available 2022-03-27T09:06:11Z
dc.date.issued 1982-01-01
dc.description.abstract Base-induced iodination of the vinylborane intermediates, conveniently obtained via the hydroboration of 1-alkynes with alkylbromoboranes (RBHBr·SMe2), provides cis-disubstituted alkenes in good yields. Muscalure, the insect pheromone of the housefly (Musca domestica), has been prepared in 59% yield. © 1982, American Chemical Society. All rights reserved.
dc.identifier.citation Journal of Organic Chemistry. v.47(19)
dc.identifier.issn 00223263
dc.identifier.uri 10.1021/jo00140a055
dc.identifier.uri https://pubs.acs.org/doi/abs/10.1021/jo00140a055
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/12418
dc.title A General and Stereospecific Synthesis of Cis Alkenes via Stepwise Hydroboration: A Simple Synthesis of Muscalure, the Sex Pheromone of the Housefly (Musca domestica)
dc.type Journal. Letter
dspace.entity.type
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