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Synthesis of bis(aryloxy)fluoromethanes using a heterodihalocarbene strategy

A side-product present in the herbicide pyroxasulfone was synthesized. The construction of a bis(aryloxy)fluoromethane moiety was necessary, for which no existing method was available. We report a simple, new procedure which we applied to the synthesis of some of these unusual structures.

Detalles Bibliográficos
Autores principales: Recsei, Carl, Barda, Yaniv
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8056069/
https://www.ncbi.nlm.nih.gov/pubmed/33936312
http://dx.doi.org/10.3762/bjoc.17.70
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author Recsei, Carl
Barda, Yaniv
author_facet Recsei, Carl
Barda, Yaniv
author_sort Recsei, Carl
collection PubMed
description A side-product present in the herbicide pyroxasulfone was synthesized. The construction of a bis(aryloxy)fluoromethane moiety was necessary, for which no existing method was available. We report a simple, new procedure which we applied to the synthesis of some of these unusual structures.
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spelling pubmed-80560692021-04-30 Synthesis of bis(aryloxy)fluoromethanes using a heterodihalocarbene strategy Recsei, Carl Barda, Yaniv Beilstein J Org Chem Letter A side-product present in the herbicide pyroxasulfone was synthesized. The construction of a bis(aryloxy)fluoromethane moiety was necessary, for which no existing method was available. We report a simple, new procedure which we applied to the synthesis of some of these unusual structures. Beilstein-Institut 2021-04-12 /pmc/articles/PMC8056069/ /pubmed/33936312 http://dx.doi.org/10.3762/bjoc.17.70 Text en Copyright © 2021, Recsei and Barda https://creativecommons.org/licenses/by/4.0/https://www.beilstein-journals.org/bjoc/terms/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) ). Please note that the reuse, redistribution and reproduction in particular requires that the author(s) and source are credited and that individual graphics may be subject to special legal provisions. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms/terms)
spellingShingle Letter
Recsei, Carl
Barda, Yaniv
Synthesis of bis(aryloxy)fluoromethanes using a heterodihalocarbene strategy
title Synthesis of bis(aryloxy)fluoromethanes using a heterodihalocarbene strategy
title_full Synthesis of bis(aryloxy)fluoromethanes using a heterodihalocarbene strategy
title_fullStr Synthesis of bis(aryloxy)fluoromethanes using a heterodihalocarbene strategy
title_full_unstemmed Synthesis of bis(aryloxy)fluoromethanes using a heterodihalocarbene strategy
title_short Synthesis of bis(aryloxy)fluoromethanes using a heterodihalocarbene strategy
title_sort synthesis of bis(aryloxy)fluoromethanes using a heterodihalocarbene strategy
topic Letter
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8056069/
https://www.ncbi.nlm.nih.gov/pubmed/33936312
http://dx.doi.org/10.3762/bjoc.17.70
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