O-directed free-radical hydrostannations of propargyl ethers, acetals, and alcohols with Ph3SnH and Et3B

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dc.contributor.authorDimopoulos, P.
dc.contributor.authorAthlan, A.
dc.contributor.authorManaviazar, S.
dc.contributor.authorGeorge, J.
dc.contributor.authorWalters, M.
dc.contributor.authorLazarides, L.
dc.contributor.authorAliev, A.
dc.contributor.authorHale, K.
dc.date.issued2005
dc.description.abstract[reaction: see text] The O-directed hydrostannation of various propargyloxy substrates is reported with Ph(3)SnH/Et(3)B.
dc.description.statementofresponsibilityPaschalis Dimopoulos, Audrey Athlan, Soraya Manaviazar, Jonathan George, Marcus Walters, Linos Lazarides, Abil E. Aliev, and Karl J. Hale
dc.identifier.citationOrganic Letters, 2005; 7(24):5369-5372
dc.identifier.doi10.1021/ol051936l
dc.identifier.issn1523-7060
dc.identifier.issn1523-7052
dc.identifier.orcidGeorge, J. [0000-0002-7330-2160]
dc.identifier.urihttp://hdl.handle.net/2440/68634
dc.language.isoen
dc.publisherAmer Chemical Soc
dc.rightsCopyright © 2005 American Chemical Society
dc.source.urihttps://doi.org/10.1021/ol051936l
dc.titleO-directed free-radical hydrostannations of propargyl ethers, acetals, and alcohols with Ph3SnH and Et3B
dc.typeJournal article
pubs.publication-statusPublished

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