Stereoselective synthesis of substituted tetrahydrofurans - identification and analysis by proton NMR and MNDO, MM2 calculations

Tarakeshwar, P. ; Iqbal, Javed ; Manogaran, S. (1991) Stereoselective synthesis of substituted tetrahydrofurans - identification and analysis by proton NMR and MNDO, MM2 calculations Tetrahedron, 47 (2). pp. 297-304. ISSN 0040-4020

Full text not available from this repository.

Official URL: http://linkinghub.elsevier.com/retrieve/pii/S00404...

Related URL: http://dx.doi.org/10.1016/S0040-4020(01)80924-8

Abstract

Methyl acetoacetate and terminal olefins react in the presence of cobalt(II) acetate and oxygen to give 5-alkyl-2-hydroxy-2-methyl-3-methoxycarbonyl tetrahydrofurans in a highly stereoselective manner. Proton NMR, semiempirical MNDO and empirical MM2 methods are used to identify the particular diastereomer and the energetics of the different isomers are discussed.

Item Type:Article
Source:Copyright of this article belongs to Elsevier Science.
ID Code:17086
Deposited On:16 Nov 2010 08:32
Last Modified:25 Jun 2012 15:12

Repository Staff Only: item control page