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

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 emphasi...

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Autores principales: Cortés, Iván, Cala, L. Javier, Bracca, Andrea B. J., Kaufman, Teodoro S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Chemistry
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9056730/
https://www.ncbi.nlm.nih.gov/pubmed/35515056
http://dx.doi.org/10.1039/d0ra06930b
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author Cortés, Iván
Cala, L. Javier
Bracca, Andrea B. J.
Kaufman, Teodoro S.
author_facet Cortés, Iván
Cala, L. Javier
Bracca, Andrea B. J.
Kaufman, Teodoro S.
author_sort Cortés, Iván
collection PubMed
description 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.
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spelling pubmed-90567302022-05-04 Furo[3,2-c]coumarins carrying carbon substituents at C-2 and/or C-3. Isolation, biological activity, synthesis and reaction mechanisms Cortés, Iván Cala, L. Javier Bracca, Andrea B. J. Kaufman, Teodoro S. RSC Adv Chemistry 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. The Royal Society of Chemistry 2020-09-10 /pmc/articles/PMC9056730/ /pubmed/35515056 http://dx.doi.org/10.1039/d0ra06930b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Cortés, Iván
Cala, L. Javier
Bracca, Andrea B. J.
Kaufman, Teodoro S.
Furo[3,2-c]coumarins carrying carbon substituents at C-2 and/or C-3. Isolation, biological activity, synthesis and reaction mechanisms
title Furo[3,2-c]coumarins carrying carbon substituents at C-2 and/or C-3. Isolation, biological activity, synthesis and reaction mechanisms
title_full Furo[3,2-c]coumarins carrying carbon substituents at C-2 and/or C-3. Isolation, biological activity, synthesis and reaction mechanisms
title_fullStr Furo[3,2-c]coumarins carrying carbon substituents at C-2 and/or C-3. Isolation, biological activity, synthesis and reaction mechanisms
title_full_unstemmed Furo[3,2-c]coumarins carrying carbon substituents at C-2 and/or C-3. Isolation, biological activity, synthesis and reaction mechanisms
title_short Furo[3,2-c]coumarins carrying carbon substituents at C-2 and/or C-3. Isolation, biological activity, synthesis and reaction mechanisms
title_sort furo[3,2-c]coumarins carrying carbon substituents at c-2 and/or c-3. isolation, biological activity, synthesis and reaction mechanisms
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9056730/
https://www.ncbi.nlm.nih.gov/pubmed/35515056
http://dx.doi.org/10.1039/d0ra06930b
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