Issue 17, 1982
From the journal:

Journal of the Chemical Society, Chemical Communications

A convenient AB-ring segment for β-rhodomycinone, β-isorhodomycinone, α2-rhodomycinone, and α-citromycinone using a novel oxygenation reaction

Charles E. Coburn,   D. Keith Anderson  and  John S. Swenton  

Abstract

An unusual bishydroxylation of 2-ethyl-5,8-dimethoxy-7-bromo-1-tetralone gives an AB-ring segment suitable for elaboration to certain anthracyclinones.

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Article information

DOI
https://doi.org/10.1039/C39820000987
Article type
Paper

J. Chem. Soc., Chem. Commun., 1982, 987-988

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A convenient AB-ring segment for β-rhodomycinone, β-isorhodomycinone, α2-rhodomycinone, and α-citromycinone using a novel oxygenation reaction

C. E. Coburn, D. K. Anderson and J. S. Swenton, J. Chem. Soc., Chem. Commun., 1982, 987 DOI: 10.1039/C39820000987

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