Allenylphosphonates/allenylphosphine oxides as intermediates/precursors for intramolecular cyclization leading to phosphorus-based indenes, indenones, benzofurans, and isochromenes

dc.contributor.author Sajna, K. V.
dc.contributor.author Kumara Swamy, K. C.
dc.date.accessioned 2022-03-27T09:51:00Z
dc.date.available 2022-03-27T09:51:00Z
dc.date.issued 2012-06-15
dc.description.abstract Utilizing internally available functional groups, a simple protocol for the efficient synthesis of phosphorus-based indenes, indenones, benzofurans, and isochromenes via intramolecular cyclization of allene intermediates/precursors is generated; the latter intermediates/precursors are conveniently obtained through aldehyde-, alkylidene-, and hydroxyl-functionalized propargyl alcohols and P III-Cl precursors. The structures of key products have been unequivocally confirmed by X-ray crystallography. © 2012 American Chemical Society.
dc.identifier.citation Journal of Organic Chemistry. v.77(12)
dc.identifier.issn 00223263
dc.identifier.uri 10.1021/jo300705f
dc.identifier.uri https://pubs.acs.org/doi/10.1021/jo300705f
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/13369
dc.title Allenylphosphonates/allenylphosphine oxides as intermediates/precursors for intramolecular cyclization leading to phosphorus-based indenes, indenones, benzofurans, and isochromenes
dc.type Journal. Article
dspace.entity.type
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