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September 23, 2008Organic LettersOpen Access

Studies on the Synthesis of Durhamycin A: Stereoselective Synthesis of a Model Aglycone

Rajan Pragani William Roush

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Abstract

A stereoselective synthesis of the model aglycone corresponding to the anti-HIV aureolic acids durhamycins A (1) and B (2) is described.

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Pragani et al. (2008) studied this question.

synapsesocial.com/papers/6a838823a9c157fc60fd6ef6 https://doi.org/10.1021/ol8018727

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Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1The Structure of Mithramycin ReinvestigatedOriginal Research · 1998 · 76 citations
2UCH9, a New Antitumor Antibiotic Produced by Streptomyces: I. Producing Organism, Fermentation Isolation and Biological Activities.In Vitro Study · 1998 · 26 citations
3UCH9, a New Antitumor Antibiotic Produced byStreptomyces. II. Structure Elucidation of UCH9 by Mass and NMR Spectroscopy.Original Research · 1998 · 17 citations
4Structure refinement of the chromomycin dimer-DNA oligomer complex in solutionOriginal Research · 1992 · 100 citations
5Solution structure of the mithramycin dimer-DNA complexOriginal Research · 1993 · 142 citations

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