Issue 8, 1984

Regiospecific total synthesis of 6-deoxyanthracyclines: 6-deoxycarminomycin

Abstract

The regiospecific synthesis of the novel anthracycline 6-deoxycarminomycin (14b)is reported: the construction of the aglycone is based on the coupling of 1,4,5-trimethoxy-3-lithionaphthlene(3) to lactone(9) in a regioselective fashion, a new synthetic approach which provides a general route to 6-deoxyanthracyclinones.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1984, 530-531

Regiospecific total synthesis of 6-deoxyanthracyclines: 6-deoxycarminomycin

F. Angelucci, F. Arcamone, G. Barchielli, A. Suarato, E. Vanotti and S. Penco, J. Chem. Soc., Chem. Commun., 1984, 530 DOI: 10.1039/C39840000530

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements