Issue 55, 2020

Furo[3,2-c]coumarins carrying carbon substituents at C-2 and/or C-3. Isolation, biological activity, synthesis and reaction mechanisms

Abstract

The isolation, biological activity and synthesis of natural furo[3,2-c]coumarins are presented, covering mainly the developments in the last 35 years. The most relevant approaches toward the synthesis of 2-substituted, 3-substituted and 2,3-disubstituted heterocycles are also discussed, with emphasis on the efficiency of the processes and their mechanisms.

Graphical abstract: Furo[3,2-c]coumarins carrying carbon substituents at C-2 and/or C-3. Isolation, biological activity, synthesis and reaction mechanisms

Article information

Article type
Review Article
Submitted
11 Aug 2020
Accepted
01 Sep 2020
First published
10 Sep 2020
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2020,10, 33344-33377

Furo[3,2-c]coumarins carrying carbon substituents at C-2 and/or C-3. Isolation, biological activity, synthesis and reaction mechanisms

I. Cortés, L. J. Cala, A. B. J. Bracca and T. S. Kaufman, RSC Adv., 2020, 10, 33344 DOI: 10.1039/D0RA06930B

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