Hanessian-Hullar reaction in the synthesis of highly substituted trans-3,4-dihydroxypyrrolidines: Rhamnulose iminosugar mimics inhibit α-glucosidase-Reference-Cited by-同舟云学术

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Hanessian-Hullar reaction in the synthesis of highly substituted trans-3,4-dihydroxypyrrolidines: Rhamnulose iminosugar mimics inhibit α-glucosidase

Published:2020-01 Issue:1 Volume:76 Page:130758
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Liu Zilei,Yoshihara Akihide,Jenkinson Sarah F.,Wormald Mark R.,Kelly Ciarán,Heap John T.,Marqvorsen Mikkel H.S.,Estévez Ramón J.,Fleet George W.J.,Nakagawa Shinpei,Izumori Ken,Nash Robert J.,Kato Atsushi

Funder

JSPS

Biotechnology and Biological Sciences Research Council

University of Kagawa

Centro Singular de Investigación de Galicia

ERDF

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference58 articles.

1. Polyhydroxylated alkaloids — natural occurrence and therapeutic applications

2. Iminosugars as therapeutic agents: recent advances and promising trends

3. Glycosidase Inhibition by All 10 Stereoisomeric 2,5-Dideoxy-2,5-iminohexitols Prepared from the Enantiomers of Glucuronolactone

4. 2-Hydroxymethyl-3,4-dihydroxy-6-methylpyrrolidine (6-Deoxy-DMDP), an Alkaloid β-Mannosidase Inhibitor from Seeds of Angylocalyx pynaertii

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Enantioselective Synthesis of 2,3,4,5‐Tetra(hydroxyalkyl)pyrrolidines through 1,3‐Dipolar Cycloadditions;European Journal of Organic Chemistry;2022-08-16

2. The Expedition of Azido-reductive Cyclization Approaches Towards Various Heterocycles;Current Organic Chemistry;2022-02

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