Novel synthetic approaches to manβ1-4GLCNAc and LeX units from N-acetyllactosamine

Article abstract of DOI:10.1080/07328309808002347

Regioselective protection of N-acetyllactosamine with triphenylmethyl (trityl) and pivaloyl groups afforded the corresponding 3, 2′, 4′-tri- and 2′,4′-dihydroxyl derivatives in a few steps, respectively; these derivatives were used efficiently for the syntheses of the title compounds from N-acetyllactosamine in 46% (7 steps) and 19% (8 steps) overall yields, respectively.

Full text of DOI:10.1080/07328309808002347

Journal of Carbohydrate Chemistry
ISSN: 0732-8303 (Print) 1532-2327 (Online) Journal homepage: http://www.tandfonline.com/loi/lcar20
Novel Synthetic Approaches to Manβ1-4GLCNAc
and Lex Units from N-Acetyllactosamine
Ken-ichi Sato , Hiroshi Seki , Akira Yoshitomo , Hiroshi Nanaumi , Yoshimitsu
Takai & Yoshiharu Ishido
To cite this article: Ken-ichi Sato , Hiroshi Seki , Akira Yoshitomo , Hiroshi Nanaumi , Yoshimitsu
Takai & Yoshiharu Ishido (1998) Novel Synthetic Approaches to Manβ1-4GLCNAc and Lex Units
from N-Acetyllactosamine , Journal of Carbohydrate Chemistry, 17:4-5, 703-727
To link to this article: http://dx.doi.org/10.1080/07328309808002347
Published online: 22 Aug 2006.
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Date: 08 June 2016, At: 20:17