Iminoheptitols as glycosidase inhibitors: Synthesis of, and mannosidase and fucosidase inhibition by, α—homomannojirimycin and 6-epi-homomannojirimycin
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference15 articles.
1. A facile, practical synthesis of 2,6-dideoxy-2,6-imino-7-O-.beta.-D-glucopyranosyl-D-glycero-L-gulo-heptitol (MDL 25,637)
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. α-Homonojirimycin [2,6-dideoxy-2,6-imino-d-glycero-l-gulo-heptitol] from omphalea diandra L.: isolation and glucosidase inhibtion
4. Iminoheptitols as glycosidase inhibitors: synthesis of and specific α-L-fucosidase inhibition by β-L-homofuconojirimycin and 1-β-C-substituted deoxymannojirimycins
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1. Divergent synthesis of various iminocyclitols from d-ribose;Organic & Biomolecular Chemistry;2015
2. An approach to 8 stereoisomers of homonojirimycin from d-glucose via kinetic & thermodynamic azido-γ-lactones;Organic & Biomolecular Chemistry;2013
3. Eight Stereoisomers of Homonojirimycin from d-Mannose;Organic Letters;2012-04-03
4. Piperidine Azasugars Displaying Competitive alpha-Rhamnosidase Inhibition and their Kinetic Mechanism;J KOREAN SOC APPL BI;2011
5. Syntheses and Biological Activities of Iminosugars as α-L-Fucosidase Inhibitors;Current Organic Synthesis;2011-02-01
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