Highly efficient O-glycosylations with p-tolyl thioribosides and p-TolSOTf. - Wikidata - wikimedia - TriplyDB

Highly efficient O-glycosylations with p-tolyl thioribosides and p-TolSOTf.

Highly efficient O-glycosylations with p-tolyl thioribosides and p-TolSOTf.

http://www.wikidata.org/entity/Q33368397

about

Synthesis of ureidomuraymycidine derivatives for structure-activity relationship studies of muraymycins.A reliable Pd-mediated hydrogenolytic deprotection of BOM group of uridine ureido nitrogen A new protecting group and linker for uridine ureido nitrogen.MILD AND SELECTIVE O-GLYCOSYLATIONS OF PRIMARY ALCOHOLS WITH THE THIOGLUCOSAMINIDE DERIVATIVE PROMOTED BY N-IODOSUCCINIMIDE AND HBF(4)-ADOSROBED ON SILICA GEL.Selective esterifications of primary alcohols in a water-containing solvent Stereocontrolled Total Synthesis of Muraymycin D1 Having a Dual Mode of Action against Mycobacterium tuberculosis.Improved synthesis of capuramycin and its analogues.Novel FR-900493 Analogues That Inhibit the Outgrowth of Clostridium difficile Spores.5'-Methylene-triazole-substituted-aminoribosyl uridines as MraY inhibitors: synthesis, biological evaluation and molecular modeling.

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P2860

Highly efficient O-glycosylations with p-tolyl thioribosides and p-TolSOTf.

http://www.wikidata.org/entity/Q33368397

description

2008 nî lūn-bûn

@nan

2008 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2008 թվականի դեկտեմբերին հրատարակված գիտական հոդված

@hy

2008年の論文

@ja

2008年学术文章

@wuu

2008年学术文章

@zh-cn

2008年学术文章

@zh-hans

2008年学术文章

@zh-my

2008年学术文章

@zh-sg

2008年學術文章

@yue

name

Highly efficient O-glycosylations with p-tolyl thioribosides and p-TolSOTf.

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Highly efficient O-glycosylations with p-tolyl thioribosides and p-TolSOTf.

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type

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Highly efficient O-glycosylations with p-tolyl thioribosides and p-TolSOTf.

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Highly efficient O-glycosylations with p-tolyl thioribosides and p-TolSOTf.

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prefLabel

Highly efficient O-glycosylations with p-tolyl thioribosides and p-TolSOTf.

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Highly efficient O-glycosylations with p-tolyl thioribosides and p-TolSOTf.

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Journal of Organic Chemistry

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Highly efficient O-glycosylations with p-tolyl thioribosides and p-TolSOTf.

@en

P2093

Kai Li

http://www.w3.org/2001/XMLSchema#string

Michio Kurosu

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P2860

Formation of the glycan chains in the synthesis of bacterial peptidoglycan

Synthesis of analogues of the O-beta-D-ribofuranosyl nucleoside moiety of liposidomycins. Part 1: contribution of the amino group and the uracil moiety upon the inhibition of MraY.

MraY Inhibitors as Novel Antibacterial Agents.

Silver(I) tetrafluoroborate as a potent promoter for chemical glycosylation

Polymer-supported (2,6-dichloro- 4-alkoxyphenyl)(2,4-dichlorophenyl)methanol: a new linker for solid-phase organic synthesis.

Disaccharide analogs as probes for glycosyltransferases in Mycobacterium tuberculosis

Thioglycosides as glycosyl donors in oligosaccharide synthesis.

Synthesis and antimycobacterial activity of capuramycin analogues. Part 2: acylated derivatives of capuramycin-related compounds.

Electrostatic interactions in cations and their importance in biology and chemistry.

Total synthesis of caprazol, a core structure of the caprazamycin antituberculosis antibiotics.

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9767-9770

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scholarly article

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10.1021/JO801408X

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24

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73

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2008-12-01T00:00:00Z

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