Highly chemoselective and stereoselective conjugate addition of benzyl copper reagents to α-oxoketene dithioacetals

Mehta, Barun K. ; Ila, Hiriyakkanavar ; Junjappa, Hiriyakkanavar (1995) Highly chemoselective and stereoselective conjugate addition of benzyl copper reagents to α-oxoketene dithioacetals Tetrahedron Letters, 36 (11). pp. 1925-1928. ISSN 0040-4039

Full text not available from this repository.

Official URL: http://linkinghub.elsevier.com/retrieve/pii/004040...

Related URL: http://dx.doi.org/10.1016/0040-4039(95)00158-9

Abstract

Benzyl copper reagents derived by transmetallation between benzylmagnesium chloride and Cu(I) species are shown to undergo conjugate addition - elimination with acyclic and cyclic α-oxoketene dithioacetals to afford the corresponding β-benzyl vinylogous thiolesters in highly stereo- and chemoselective manner.

Item Type:Article
Source:Copyright of this article belongs to Elsevier Science.
ID Code:15325
Deposited On:13 Nov 2010 12:56
Last Modified:22 Feb 2011 08:29

Repository Staff Only: item control page