Issue 16, 1984

Stereocontrol at ‘off-temple’ sites in 1,2-O-isopropylidene glycofuranoses

Abstract

Hydrogenation of the double bond at C(5) of diester (12) occurs exclusively from the si-si face provided that a bulky substituent is present at C(3) in cis relationship to the olefinic side chain.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1984, 1122-1123

Stereocontrol at ‘off-temple’ sites in 1,2-O-isopropylidene glycofuranoses

M. Georges, T. F. Tam and B. Fraser-Reid, J. Chem. Soc., Chem. Commun., 1984, 1122 DOI: 10.1039/C39840001122

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements