SYNTHETIC APPROACH TO TETRAHYDROFURAN UNITS AND FIVE-MEMBERED RING LACTONES FUSED TO HEXOPYRANOSIDES *-Reference-Cited by-同舟云学术

SYNTHETIC APPROACH TO TETRAHYDROFURAN UNITS AND FIVE-MEMBERED RING LACTONES FUSED TO HEXOPYRANOSIDES *

Published:2002-09-23 Issue:4 Volume:21 Page:257-273
ISSN:0732-8303
Container-title:Journal of Carbohydrate Chemistry
language:en
Short-container-title:Journal of Carbohydrate Chemistry

Author:

Rauter Amélia P.¹,Oliveira Olga¹,Canda Tana¹,Leroi Estelle²,Ferreira Humberto³,Ferreira Maria J.³,Ascenso José A.³

Affiliation:

1. a Departamento de Química e Bioquímica da Faculdade de Ciências da Universidade de Lisboa , Edifício C8, 5° Piso, Campo Grande, Lisboa, 1749-016, Portugal

2. b Institut Universitaire de Technologie de Poitiers , France

3. c Centro de Química Estrutural do Instituto Superior Técnico , Av. Rovisco Pais, Lisboa, Portugal

Publisher

Informa UK Limited

Subject

Organic Chemistry,Biochemistry

Link

https://www.tandfonline.com/doi/pdf/10.1081/CAR-120013489

Reference18 articles.

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

2. Construction of a branched chain at C-3 of a hexopyranoside. Synthesis of miharamycin sugar moiety analogs

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

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