Iminoheptitols as glycosidase inhibitors: synthesis of and specific α-L-fucosidase inhibition by β-L-homofuconojirimycin and 1-β-C-substituted deoxymannojirimycins-Reference-Cited by-同舟云学术

Iminoheptitols as glycosidase inhibitors: synthesis of and specific α-L-fucosidase inhibition by β-L-homofuconojirimycin and 1-β-C-substituted deoxymannojirimycins

Published:1989-01 Issue:33 Volume:30 Page:4439-4442
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Fleet G.W.J.,Namgoong S.K.,Barker C.,Baines S.,Jacob G.S.,Winchester B.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference16 articles.

1. α-Homonojirimycin [2,6-dideoxy-2,6-imino-d-glycero-l-gulo-heptitol] from omphalea diandra L.: isolation and glucosidase inhibtion

2. Total synthesis of 2,6-dideoxy-2,6-imino-7-O-(.beta.-D-glucopyranosyl)-D-glycero-L-gulo-heptitol hydrochloride. A potent inhibitor of .alpha.-glucosidases

3. Short efficient synthesis of the α-L-fucosidase inhibitor, deoxyfuconojirimycin [1,5-dideoxy-1,5-imino-L-fucitol] fromD-lyxonolactone

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