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Decarboxylative aldol reaction of α,α-difluoro-β-ketocarboxylate salt: a facile method for generation of difluoroenolate

We developed a decarboxylative aldol reaction using α,α-difluoro-β-ketocarboxylate salt, carbonyl compounds, and ZnCl(2)/N,N,N′,N′-tetramethylethylenediamine. The generation of difluoroenolate proceeded smoothly under mild heating to provide α,α-difluoro-β-hydroxy ketones in good to excellent yield...

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Detalles Bibliográficos
Autores principales: Tarui, Atsushi, Oduti, Mayuna, Shinya, Susumu, Sato, Kazuyuki, Omote, Masaaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9080823/
https://www.ncbi.nlm.nih.gov/pubmed/35542341
http://dx.doi.org/10.1039/c8ra02440e
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author Tarui, Atsushi
Oduti, Mayuna
Shinya, Susumu
Sato, Kazuyuki
Omote, Masaaki
author_facet Tarui, Atsushi
Oduti, Mayuna
Shinya, Susumu
Sato, Kazuyuki
Omote, Masaaki
author_sort Tarui, Atsushi
collection PubMed
description We developed a decarboxylative aldol reaction using α,α-difluoro-β-ketocarboxylate salt, carbonyl compounds, and ZnCl(2)/N,N,N′,N′-tetramethylethylenediamine. The generation of difluoroenolate proceeded smoothly under mild heating to provide α,α-difluoro-β-hydroxy ketones in good to excellent yield (up to 99%). The α,α-difluoro-β-ketocarboxylate salt was bench stable and easy to handle under air, which realizes a convenient and environmentally friendly methodology for synthesis of difluoromethylene compounds.
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spelling pubmed-90808232022-05-09 Decarboxylative aldol reaction of α,α-difluoro-β-ketocarboxylate salt: a facile method for generation of difluoroenolate Tarui, Atsushi Oduti, Mayuna Shinya, Susumu Sato, Kazuyuki Omote, Masaaki RSC Adv Chemistry We developed a decarboxylative aldol reaction using α,α-difluoro-β-ketocarboxylate salt, carbonyl compounds, and ZnCl(2)/N,N,N′,N′-tetramethylethylenediamine. The generation of difluoroenolate proceeded smoothly under mild heating to provide α,α-difluoro-β-hydroxy ketones in good to excellent yield (up to 99%). The α,α-difluoro-β-ketocarboxylate salt was bench stable and easy to handle under air, which realizes a convenient and environmentally friendly methodology for synthesis of difluoromethylene compounds. The Royal Society of Chemistry 2018-06-05 /pmc/articles/PMC9080823/ /pubmed/35542341 http://dx.doi.org/10.1039/c8ra02440e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Tarui, Atsushi
Oduti, Mayuna
Shinya, Susumu
Sato, Kazuyuki
Omote, Masaaki
Decarboxylative aldol reaction of α,α-difluoro-β-ketocarboxylate salt: a facile method for generation of difluoroenolate
title Decarboxylative aldol reaction of α,α-difluoro-β-ketocarboxylate salt: a facile method for generation of difluoroenolate
title_full Decarboxylative aldol reaction of α,α-difluoro-β-ketocarboxylate salt: a facile method for generation of difluoroenolate
title_fullStr Decarboxylative aldol reaction of α,α-difluoro-β-ketocarboxylate salt: a facile method for generation of difluoroenolate
title_full_unstemmed Decarboxylative aldol reaction of α,α-difluoro-β-ketocarboxylate salt: a facile method for generation of difluoroenolate
title_short Decarboxylative aldol reaction of α,α-difluoro-β-ketocarboxylate salt: a facile method for generation of difluoroenolate
title_sort decarboxylative aldol reaction of α,α-difluoro-β-ketocarboxylate salt: a facile method for generation of difluoroenolate
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9080823/
https://www.ncbi.nlm.nih.gov/pubmed/35542341
http://dx.doi.org/10.1039/c8ra02440e
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