Deoxygenation at C-4 and Stereospecific Branched-Chain Construction at C-3 of a Methyl Hexopyranuloside. Synthetic Approach to the Amipurimycin Sugar Moiety-Reference-Cited by-同舟云学术

Deoxygenation at C-4 and Stereospecific Branched-Chain Construction at C-3 of a Methyl Hexopyranuloside. Synthetic Approach to the Amipurimycin Sugar Moiety

Published:1996-01-01 Issue:11 Volume:61 Page:3594-3598
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Rauter Amélia P.¹,Fernandes Ana C.¹,Czernecki Stanislas¹,Valery Jean-Marc¹

Affiliation:

1. Departamento de Química e Bioquímica, Faculdade de Ciências, Universidade de Lisboa, Edifício C1, 5° Piso, Campo Grande, 1700 Lisboa, Portugal, and Laboratoire de Chimie des Glucides, Université Pierre et Marie Curie, 4 Place Jussieu, 75005 Paris, France

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo952220e

Reference26 articles.

1. Isolation and characterization of a new nucleoside antibiotic, amipurimycin.

2. Streptomyces novoguineensis sp. nov., an amipurimycin producer, and antimicrobial activity of amipurimycin.

3. Structure of amipurimycin, a nucleoside antibiotic having a novel branched sugar moiety

4. Synthesis of methyl 4-deoxy-3-C-[(S)-1,2-dihydroxyethyl]-α-d-xylo-hexopyranoside and methyl 2,2′-anhydro-3-C-[(S)-1,2-dihydroxyethyl]-α-d-glucopyranoside derivatives

5. Reaktionen partiell acylierter Aldohexopyranoside, II. Regioselektive Oxidatin partiell acylierter Aldohexopyranoside mit Pyridiniumchlorochromat und ein neues photochemisches Verfahren zur Darstellung von Methyl-3,6-didesoxy-α-D-ribo- hexopyranosid

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