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Synthesis of Phthalides and α,β-butenolides by Transition Metal-Catalyzed Activation of C—H Bonds

Phthalides and α,β-butenolides are two related classes of oxygenated heterocycles with a wide range of biological activities. An innovative strategy to prepare these compounds is based on C—H bond functionalization reactions, in which two simple, unfunctionalized molecules are coupled together with...

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Detalles Bibliográficos
Autores principales: Renzetti, Andrea, Fukumoto, Kozo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6412913/
https://www.ncbi.nlm.nih.gov/pubmed/30823615
http://dx.doi.org/10.3390/molecules24040824
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author Renzetti, Andrea
Fukumoto, Kozo
author_facet Renzetti, Andrea
Fukumoto, Kozo
author_sort Renzetti, Andrea
collection PubMed
description Phthalides and α,β-butenolides are two related classes of oxygenated heterocycles with a wide range of biological activities. An innovative strategy to prepare these compounds is based on C—H bond functionalization reactions, in which two simple, unfunctionalized molecules are coupled together with cleavage of a C—H bond and formation of a C—X bond (X=C or heteroatom). This paper reviews the methods for the synthesis of phthalides and α,β-butenolides by C—H bond functionalization from non-halogenated starting materials. Over 30 methods are reported, mostly developed during the past ten years.
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spelling pubmed-64129132019-04-09 Synthesis of Phthalides and α,β-butenolides by Transition Metal-Catalyzed Activation of C—H Bonds Renzetti, Andrea Fukumoto, Kozo Molecules Review Phthalides and α,β-butenolides are two related classes of oxygenated heterocycles with a wide range of biological activities. An innovative strategy to prepare these compounds is based on C—H bond functionalization reactions, in which two simple, unfunctionalized molecules are coupled together with cleavage of a C—H bond and formation of a C—X bond (X=C or heteroatom). This paper reviews the methods for the synthesis of phthalides and α,β-butenolides by C—H bond functionalization from non-halogenated starting materials. Over 30 methods are reported, mostly developed during the past ten years. MDPI 2019-02-25 /pmc/articles/PMC6412913/ /pubmed/30823615 http://dx.doi.org/10.3390/molecules24040824 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Renzetti, Andrea
Fukumoto, Kozo
Synthesis of Phthalides and α,β-butenolides by Transition Metal-Catalyzed Activation of C—H Bonds
title Synthesis of Phthalides and α,β-butenolides by Transition Metal-Catalyzed Activation of C—H Bonds
title_full Synthesis of Phthalides and α,β-butenolides by Transition Metal-Catalyzed Activation of C—H Bonds
title_fullStr Synthesis of Phthalides and α,β-butenolides by Transition Metal-Catalyzed Activation of C—H Bonds
title_full_unstemmed Synthesis of Phthalides and α,β-butenolides by Transition Metal-Catalyzed Activation of C—H Bonds
title_short Synthesis of Phthalides and α,β-butenolides by Transition Metal-Catalyzed Activation of C—H Bonds
title_sort synthesis of phthalides and α,β-butenolides by transition metal-catalyzed activation of c—h bonds
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6412913/
https://www.ncbi.nlm.nih.gov/pubmed/30823615
http://dx.doi.org/10.3390/molecules24040824
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