Conversion of propargyl alcohols to chloroallenes and arylalkynes using the TiCl < inf > 4 < /inf > /R < inf > 3 < /inf > N reagent system

dc.contributor.author Karunakar, Galla V.
dc.contributor.author Periasamy, Mariappan
dc.date.accessioned 2022-03-27T09:08:19Z
dc.date.available 2022-03-27T09:08:19Z
dc.date.issued 2006-09-15
dc.description.abstract Whereas the reaction of certain propargyl alcohols with TiCl4 in the presence of tertiary alkylamines gives the corresponding chloroallenes in 37-58% yields, reaction with the tertiary arylamines gives the corresponding arylalkynes in 68-77% yields. © 2006 American Chemical Society.
dc.identifier.citation Journal of Organic Chemistry. v.71(19)
dc.identifier.issn 00223263
dc.identifier.uri 10.1021/jo060683m
dc.identifier.uri https://pubs.acs.org/doi/10.1021/jo060683m
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/12476
dc.title Conversion of propargyl alcohols to chloroallenes and arylalkynes using the TiCl < inf > 4 < /inf > /R < inf > 3 < /inf > N reagent system
dc.type Journal. Article
dspace.entity.type
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