Furo[3,2-c]coumarins carrying carbon substituents at C-2 and/or C-3. Isolation, biological activity, synthesis and reaction mechanisms-Reference-Cited by-同舟云学术

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

Published:2020 Issue:55 Volume:10 Page:33344-33377
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Cortés Iván¹²³⁴^ORCID,Cala L. Javier¹²³⁴,Bracca Andrea B. J.¹²³⁴^ORCID,Kaufman Teodoro S.¹²³⁴^ORCID

Affiliation:

1. Instituto de Química Rosario (IQUIR, CONICET-UNR)

2. Facultad de Ciencias Bioquímicas y Farmacéuticas – Universidad Nacional de Rosario

3. S2002LRK Rosario

4. Argentina

Abstract

The isolation, synthesis and biological activity of naturally occurring furo[3,2-c] coumarins carrying carbon substituents at C-2 and/or C-3, is discussed. Synthetic approaches toward the properly functionalized heterocyclic motif are also presented.

Funder

Fondo para la Investigación Científica y Tecnológica

Consejo Nacional de Investigaciones Científicas y Técnicas

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2020/RA/D0RA06930B

Reference317 articles.

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4. Syntheses of furo[3,4-c]coumarins and related furyl coumarin derivatives via intramolecular Wittig reactions

5. First synthesis of furo[3,4-c]coumarins

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