Synthesis of an α-mannosidase inhibitor, (±)-mannostatin A and its isomer-Reference-Cited by-同舟云学术

Synthesis of an α-mannosidase inhibitor, (±)-mannostatin A and its isomer

Published:1991 Issue:13 Volume: Page:890-891
ISSN:0022-4936
Container-title:J. Chem. Soc., Chem. Commun.
language:en
Short-container-title:J. Chem. Soc., Chem. Commun.

Author:

Ogawa Seiichiro,Yuming Yu

Publisher

Royal Society of Chemistry (RSC)

Subject

Molecular Medicine

Link

http://pubs.rsc.org/en/content/articlepdf/1991/C3/C39910000890

Reference8 articles.

1. Mannostatins A and B: New inhibitors of .ALPHA.-D-mannosidase, produced by Stereptoverticillium verticillus var. quintum ME3-AG3: Taxonomy, production, isolation, physico-chemical properties and biological activities.

2. Structure determination of mannostatins A and B.

3. In this paper, nomenclature of cyclitols follows IUPAC-IUB 1973 Recommendations for Cyclitol[Pure Appl. Chem., 1974, 37, 285]. The stereochemical feature of cyclitols is shown by a fractional notation whereby numerals in the numerator denote hydroxy or other groups above the plane of the ring while numerals in the denominator denote hydroxy or other groups below that plane.

4. Synthesis and biological activities of methyl oligobiosaminide and some deoxy isomers thereof

5. 804. Cyclitols. Part IX. Cyclohexylidene derivatives of myoinositol

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