New Stereodivergent Approach to 3-Amino-2,3,6-trideoxysugars. Enantioselective Synthesis of Daunosamine, Ristosamine, Acosamine, and Epi-daunosamine-Reference-Cited by-同舟云学术

New Stereodivergent Approach to 3-Amino-2,3,6-trideoxysugars. Enantioselective Synthesis of Daunosamine, Ristosamine, Acosamine, and Epi-daunosamine

Published:2003-07-19 Issue:17 Volume:5 Page:3001-3004
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Ginesta Xavier¹,Pastó Mireia¹,Pericàs Miquel A.¹,Riera Antoni¹

Affiliation:

1. Unitat de Recerca en Síntesi Asimètrica (URSA-PCB), Departament de Química Orgànica/Parc Científic de Barcelona, Universitat de Barcelona, C/Josep Samitier 1-5, 08028 Barcelona, Spain

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol034843h

Reference33 articles.

1. Synthesis and biological evaluation of some 14-O-acyl derivatives of adriamycin

2. Daunomycin. II. The Structure and Stereochemistry of Daunosamine

3. Synthesis and antitumor properties of new glycosides of daunomycinone and adriamycinone

4. A short and efficient transformation of rhamnose into activated daunosamine, acosamine, ristosamine and epi-daunosamine derivatives, and synthesis of an anthracycline antibiotic acosaminyl-ε-iso-rhodomycinone

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