Functionalization at Proanomeric Centres by Photobromination. A Novel Access to Oxo- and Acyloxyimino-glycosyl Bromides-Reference-Cited by-同舟云学术

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Functionalization at Proanomeric Centres by Photobromination. A Novel Access to Oxo- and Acyloxyimino-glycosyl Bromides

Published:1982 Issue:S8 Volume:21 Page:1449-1459
ISSN:0570-0833
Container-title:Angewandte Chemie International Edition in English
language:en
Short-container-title:Angew. Chem. Int. Ed. Engl.

Author:

Lichtenthaler Frieder W.,Jarglis Pan

Publisher

Wiley

Subject

General Chemistry,Catalysis

Reference36 articles.

1. Eine stereospezifische Synthese von (S,S)-Palythazin aus D-Glucose

2. Angew. Chem. suppl. (1982) 175.

3. Chemistry of the O-Glycosidic Bond, Pergamon Press, Oxford/New York 1979.

4. Di-carbonyl-Zucker. II. Über ein neues Oxydationsprodukt der Glucose.

Cited by 9 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. 4,6-di-O-benzoyl-3-O-benzyl-α-d-arabino-hexopyranos-2-ulosyl bromide: A conveniently accessible glycosyl donor for the expedient construction of diantennary β-d-mannosides branched at O-3 and O-6;Carbohydrate Research;1997-12

2. Synthesis and some transformations of 1-azido-glycopyranosyl cyanides-precursors of anomeric α-amino acids;Tetrahedron;1996-07

3. Preparation of acetylated 2,6-anhydrohept(hex)-2-enono-nitriles (1-cyano-2-hydroxyglycals);Carbohydrate Research;1991-04

4. Radical-Mediated Brominations at Ring Positions of Carbohydrates;Advances in Carbohydrate Chemistry and Biochemistry;1991

5. Photohalogenation of glycopyranosyl halides: An expedient route to c-1 gem dihalogenated sugars;Tetrahedron;1989-01

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