Novel regio- and stereoselective phosphonyl radical addition to glycals promoted by Mn(ii)–air: syntheses of 1,2-dideoxy 2-C-diphenylphosphinylglycopyranosides-Reference-Cited by-同舟云学术

Novel regio- and stereoselective phosphonyl radical addition to glycals promoted by Mn(ii)–air: syntheses of 1,2-dideoxy 2-C-diphenylphosphinylglycopyranosides

Published:2014 Issue:16 Volume:50 Page:2046-2048
ISSN:1359-7345
Container-title:Chem. Commun.
language:en
Short-container-title:Chem. Commun.

Author:

Zhang Fuyi¹²³⁴,Wang Liming¹²³⁴,Zhang Cui¹²³⁴,Zhao Yufen¹²³⁴⁵

Affiliation:

1. The College of Chemistry and Molecular Engineering

2. The Key Lab of Chemical Biology and Organic Chemistry

3. Zhengzhou University

4. Zhengzhou 450052, China

5. College of Chemistry and Chemical Engineering

Abstract

The novel Mn(ii)–air promoted radical reaction of diphenylphosphine oxide with various glycals in excellent regio- and stereoselectivities generated 1,2-dideoxy-2-C-diphenylphosphinylglycopyranosides.

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2014/CC/C3CC48806C

Reference57 articles.

1. Synthesis of glycosyl phosphonates and related compounds

2. Synthesis of Glycosylphosphine Oxides and Related Compounds

3. Novel UDP-Glycal Derivatives as Transition State Analogue Inhibitors of UDP-GlcNAc 2-Epimerase

4. Synthesis of a Ring-Oxygenated Variant of the 2-Carboxy-6-hydroxyoctahydroindole Core of Aeruginosin 298-A from Glucose

5. Artificial N-functionalized UDP-glucosamine analogues as modified substrates for N-acetylglucosaminyl transferases

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