Enantioselective synthesis of functionalized 1-benzoxepines by phenoxide ion-mediated 7-endo-tet carbocyclization of cyclic sulfates

Das, S K; Dinda, S K; Panda, Gautam

dc.contributor.author	Das, S K
dc.contributor.author	Dinda, S K
dc.contributor.author	Panda, Gautam
dc.date.accessioned	2010-09-09T08:51:50Z
dc.date.available	2010-09-09T08:51:50Z
dc.date.issued	2009
dc.identifier.citation	Eur. J. Org. Chem. 2009(2), 204-207	en
dc.identifier.uri	http://hdl.handle.net/123456789/585
dc.description.abstract	Asymmetric synthesis of 2,3-disubstituted-1-benzoxepines is described. Key steps include Sharpless asymmetric dihydroxylation of trans-α,β-unsaturated esters and phenoxide ion-mediated intramolecular 7-endo-tet carbocyclization of syn-2,3-dihydroxy ester-derived cyclic sulphates.	en
dc.format.extent	164191 bytes
dc.format.mimetype	application/pdf
dc.language.iso	en	en
dc.subject	1-Benzoxepine	en
dc.subject	Sharpless asymmetric dihydroxylation	en
dc.subject	Cyclic sulphate	en
dc.title	Enantioselective synthesis of functionalized 1-benzoxepines by phenoxide ion-mediated 7-endo-tet carbocyclization of cyclic sulfates	en
dc.type	Article	en