Synlett 1999; 1999(11): 1817-1819
DOI: 10.1055/s-1999-2928
letter
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.

Selectively Deprotectable Carbohydrates Based on Regioselective Enzymatic Reactions

Roland Pfau* , Horst Kunz
  • *Institut für Organische Chemie, Joh. Gutenberg-Universität Mainz, Duesbergweg 10-14, D-55128 Mainz, Germany; Fax +49-61 31-39-47 86; E-mail: hokunz@mail.uni-mainz.de
Further Information

Publication History

Publication Date:
31 December 1999 (online)

Galactals and 2-azido-2-deoxy-galactopyranosides equipped with a set of selectively removable hydroxy protecting groups are synthesized on the basis of lipase-catalyzed regioselective deacylation and acylation reactions.

    >