Cookies on this website
We use cookies to ensure that we give you the best experience on our website. If you click 'Continue' we'll assume that you are happy to receive all cookies and you won't see this message again. Click 'Find out more' for information on how to change your cookie settings.

Glycosylation reactions performed between a glycosyl donor and acceptor covalently linked to a peptide template both in the solution and solid phase give similar yields and product distributions. The adoption of a solid phase approach opens the way for the synthesis of libraries of peptide templates in an attempt to screen for particular peptide sequences that effect complete regio-and stereochemical control during glycosidic bond formation, whilst the use of second generation donors allows the possibility of an iterative approach. © 2003 Elsevier Science Ltd. All rights reserved.

Original publication

DOI

10.1016/S0957-4166(03)00118-6

Type

Journal article

Journal

Tetrahedron Asymmetry

Publication Date

02/05/2003

Volume

14

Pages

1201 - 1210