Preparation of the 4-ethylamino sugar of calicheamicin: Assignment of absolute configuration.
- 31 December 1990
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 31 (1) , 21-22
- https://doi.org/10.1016/s0040-4039(00)94323-5
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- A core system that simulates the cycloaromatization and DNA cleavage properties of calicheamicin-esperamicin: a correlation experimentThe Journal of Organic Chemistry, 1989
- Calicheamicin γ 1 I and DNA: Molecular Recognition Process Responsible for Site-SpecificityScience, 1989
- DNA cleavage by a synthetic mimic of the calicheamicin-esperamicin class of antibioticsJournal of the American Chemical Society, 1988
- Calicheamicin γ 1 I : an Antitumor Antibiotic That Cleaves Double-Stranded DNA Site SpecificallyScience, 1988
- A model for the proposed mechanism of action of the potent antitumor antibiotic esperamicin A1Journal of the American Chemical Society, 1988
- Synthesis of the bicyclic core of the esperamicin/calichemicin class of antitumor agentsJournal of the American Chemical Society, 1988
- Calichemicins, a novel family of antitumor antibiotics. 1. Chemistry and partial structure of calichemicin .gamma.1IJournal of the American Chemical Society, 1987
- Stereodivergent synthesis of threo and erythro 6-amino-6-deoxyheptosulose derivatives via an optically active oxazolidine aldehydeThe Journal of Organic Chemistry, 1986
- Cram rule selectivity in the Lewis acid catalyzed cyclocondensation of chiral aldehydes. A convenient route to chiral systems of biological interestThe Journal of Organic Chemistry, 1982
- Reactive 1,4-dehydroaromaticsAccounts of Chemical Research, 1973