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Convenient Synthesis of Functionalized Cyclopropa[c]coumarin-1a-carboxylates
A simple method has been developed for the synthesis of cyclopropa[c]coumarins, which belong to the donor-acceptor cyclopropane family and, therefore, are promising substrates for the preparation of chromene-based fine chemicals. The method, based on the acetic acid-induced intramolecular transester...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6337311/ https://www.ncbi.nlm.nih.gov/pubmed/30586901 http://dx.doi.org/10.3390/molecules24010057 |
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author | Ivanova, Olga A. Andronov, Vladimir A. Levina, Irina I. Chagarovskiy, Alexey O. Voskressensky, Leonid G. Trushkov, Igor V. |
author_facet | Ivanova, Olga A. Andronov, Vladimir A. Levina, Irina I. Chagarovskiy, Alexey O. Voskressensky, Leonid G. Trushkov, Igor V. |
author_sort | Ivanova, Olga A. |
collection | PubMed |
description | A simple method has been developed for the synthesis of cyclopropa[c]coumarins, which belong to the donor-acceptor cyclopropane family and, therefore, are promising substrates for the preparation of chromene-based fine chemicals. The method, based on the acetic acid-induced intramolecular transesterification of 2-arylcyclopropane-1,1-dicarboxylates, was found to be efficient for substrates containing hydroxy group directly attached to the aromatic ring. |
format | Online Article Text |
id | pubmed-6337311 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-63373112019-01-25 Convenient Synthesis of Functionalized Cyclopropa[c]coumarin-1a-carboxylates Ivanova, Olga A. Andronov, Vladimir A. Levina, Irina I. Chagarovskiy, Alexey O. Voskressensky, Leonid G. Trushkov, Igor V. Molecules Communication A simple method has been developed for the synthesis of cyclopropa[c]coumarins, which belong to the donor-acceptor cyclopropane family and, therefore, are promising substrates for the preparation of chromene-based fine chemicals. The method, based on the acetic acid-induced intramolecular transesterification of 2-arylcyclopropane-1,1-dicarboxylates, was found to be efficient for substrates containing hydroxy group directly attached to the aromatic ring. MDPI 2018-12-24 /pmc/articles/PMC6337311/ /pubmed/30586901 http://dx.doi.org/10.3390/molecules24010057 Text en © 2018 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 | Communication Ivanova, Olga A. Andronov, Vladimir A. Levina, Irina I. Chagarovskiy, Alexey O. Voskressensky, Leonid G. Trushkov, Igor V. Convenient Synthesis of Functionalized Cyclopropa[c]coumarin-1a-carboxylates |
title | Convenient Synthesis of Functionalized Cyclopropa[c]coumarin-1a-carboxylates |
title_full | Convenient Synthesis of Functionalized Cyclopropa[c]coumarin-1a-carboxylates |
title_fullStr | Convenient Synthesis of Functionalized Cyclopropa[c]coumarin-1a-carboxylates |
title_full_unstemmed | Convenient Synthesis of Functionalized Cyclopropa[c]coumarin-1a-carboxylates |
title_short | Convenient Synthesis of Functionalized Cyclopropa[c]coumarin-1a-carboxylates |
title_sort | convenient synthesis of functionalized cyclopropa[c]coumarin-1a-carboxylates |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6337311/ https://www.ncbi.nlm.nih.gov/pubmed/30586901 http://dx.doi.org/10.3390/molecules24010057 |
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