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Amine-Catalyzed Decarboxylative Aldol Reaction of β-Ketocarboxylic Acids with Trifluoropyruvates

Decarboxylative aldol reaction of aliphatic carboxylic acids is a useful method for C–C bond formation because carboxylic acids are an easily available class of compounds. In this study, we found that the decarboxylative aldol reaction of tertiary β-ketocarboxylic acids and trifluoropyruvates procee...

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Autores principales: Kawanishi, Ryouta, Hattori, Shinya, Iwasa, Seiji, Shibatomi, Kazutaka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6695914/
https://www.ncbi.nlm.nih.gov/pubmed/31366138
http://dx.doi.org/10.3390/molecules24152773
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author Kawanishi, Ryouta
Hattori, Shinya
Iwasa, Seiji
Shibatomi, Kazutaka
author_facet Kawanishi, Ryouta
Hattori, Shinya
Iwasa, Seiji
Shibatomi, Kazutaka
author_sort Kawanishi, Ryouta
collection PubMed
description Decarboxylative aldol reaction of aliphatic carboxylic acids is a useful method for C–C bond formation because carboxylic acids are an easily available class of compounds. In this study, we found that the decarboxylative aldol reaction of tertiary β-ketocarboxylic acids and trifluoropyruvates proceeded smoothly to yield the corresponding aldol products in high yields and with high diastereoselectivity in the presence of a tertiary amine catalyst. In this reaction, we efficiently constructed a quaternary carbon center and an adjacent trifluoromethylated carbon center. This protocol was also extended to an enantioselective reaction with a chiral amine catalyst, and the desired product was obtained with up to 73% enantioselectivity.
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spelling pubmed-66959142019-09-05 Amine-Catalyzed Decarboxylative Aldol Reaction of β-Ketocarboxylic Acids with Trifluoropyruvates Kawanishi, Ryouta Hattori, Shinya Iwasa, Seiji Shibatomi, Kazutaka Molecules Communication Decarboxylative aldol reaction of aliphatic carboxylic acids is a useful method for C–C bond formation because carboxylic acids are an easily available class of compounds. In this study, we found that the decarboxylative aldol reaction of tertiary β-ketocarboxylic acids and trifluoropyruvates proceeded smoothly to yield the corresponding aldol products in high yields and with high diastereoselectivity in the presence of a tertiary amine catalyst. In this reaction, we efficiently constructed a quaternary carbon center and an adjacent trifluoromethylated carbon center. This protocol was also extended to an enantioselective reaction with a chiral amine catalyst, and the desired product was obtained with up to 73% enantioselectivity. MDPI 2019-07-30 /pmc/articles/PMC6695914/ /pubmed/31366138 http://dx.doi.org/10.3390/molecules24152773 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 Communication
Kawanishi, Ryouta
Hattori, Shinya
Iwasa, Seiji
Shibatomi, Kazutaka
Amine-Catalyzed Decarboxylative Aldol Reaction of β-Ketocarboxylic Acids with Trifluoropyruvates
title Amine-Catalyzed Decarboxylative Aldol Reaction of β-Ketocarboxylic Acids with Trifluoropyruvates
title_full Amine-Catalyzed Decarboxylative Aldol Reaction of β-Ketocarboxylic Acids with Trifluoropyruvates
title_fullStr Amine-Catalyzed Decarboxylative Aldol Reaction of β-Ketocarboxylic Acids with Trifluoropyruvates
title_full_unstemmed Amine-Catalyzed Decarboxylative Aldol Reaction of β-Ketocarboxylic Acids with Trifluoropyruvates
title_short Amine-Catalyzed Decarboxylative Aldol Reaction of β-Ketocarboxylic Acids with Trifluoropyruvates
title_sort amine-catalyzed decarboxylative aldol reaction of β-ketocarboxylic acids with trifluoropyruvates
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6695914/
https://www.ncbi.nlm.nih.gov/pubmed/31366138
http://dx.doi.org/10.3390/molecules24152773
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