Stereoselective synthesis of tri- and tetrasubstituted oxepanes via n-Bu3SnH mediated 7-endo-trig vinyl radical cyclisation

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DC Field	Value	Language
dc.contributor.author	Shanmugam, P	-
dc.contributor.author	Rajasingh, P	-
dc.date.accessioned	2021-02-08T11:13:06Z	-
dc.date.available	2021-02-08T11:13:06Z	-
dc.date.issued	2005	-
dc.identifier.citation	Tetrahedron Letters 46(19):3369–3372; 9 May 2005	en_US
dc.identifier.issn	0040-4039	-
dc.identifier.uri	http://hdl.handle.net/123456789/3646	-
dc.description.abstract	A stereoselective 7-endo-trig cyclisation of homopropargyl and phenyl homopropargyl] derivatives of Baylis-Hillman adducts using n-Bu3SnH/AlBN mediated vinyl radical cyclisation affords tri- and tetrasubstituted oxepanes, respectively, in good yields.	en_US
dc.language.iso	en	en_US
dc.publisher	Pergamon-Elsevier Science	en_US
dc.subject	7-endo-trig	en_US
dc.subject	Vinyl radical	en_US
dc.subject	Baylis–Hillman adduct	en_US
dc.subject	Oxepanes	en_US
dc.subject	n-Butyltin hydride	en_US
dc.title	Stereoselective synthesis of tri- and tetrasubstituted oxepanes via n-Bu3SnH mediated 7-endo-trig vinyl radical cyclisation	en_US
dc.type	Article	en_US
Appears in Collections:	2005

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