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Palladium-Catalyzed One-Pot Approach to 3-(Diarylmethylene)oxindoles from Propiolamidoaryl Triflate

3-(Diarylmethylene)oxindoles have been synthesized from propiolamidoaryl triflate utilizing a palladium-catalyzed one-pot reaction consisting of three successive reactions: Sonogashira, Heck, and Suzuki-Miyaura. This method allows for the production of a complex skeleton of 3-(diarylmethylene)oxindo...

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Autores principales: Lee, Dahye, Park, Sunhwa, Yu, Yoseb, Shin, Kye Jung, Seo, Jae Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6331821/
https://www.ncbi.nlm.nih.gov/pubmed/26247925
http://dx.doi.org/10.3390/molecules200814022
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author Lee, Dahye
Park, Sunhwa
Yu, Yoseb
Shin, Kye Jung
Seo, Jae Hong
author_facet Lee, Dahye
Park, Sunhwa
Yu, Yoseb
Shin, Kye Jung
Seo, Jae Hong
author_sort Lee, Dahye
collection PubMed
description 3-(Diarylmethylene)oxindoles have been synthesized from propiolamidoaryl triflate utilizing a palladium-catalyzed one-pot reaction consisting of three successive reactions: Sonogashira, Heck, and Suzuki-Miyaura. This method allows for the production of a complex skeleton of 3-(diarylmethylene)oxindole from propiolamidoaryl triflate using a commercially available aryl iodide and arylboronic acid in a simple and efficient way with moderate yield and stereoselectivity.
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spelling pubmed-63318212019-01-24 Palladium-Catalyzed One-Pot Approach to 3-(Diarylmethylene)oxindoles from Propiolamidoaryl Triflate Lee, Dahye Park, Sunhwa Yu, Yoseb Shin, Kye Jung Seo, Jae Hong Molecules Article 3-(Diarylmethylene)oxindoles have been synthesized from propiolamidoaryl triflate utilizing a palladium-catalyzed one-pot reaction consisting of three successive reactions: Sonogashira, Heck, and Suzuki-Miyaura. This method allows for the production of a complex skeleton of 3-(diarylmethylene)oxindole from propiolamidoaryl triflate using a commercially available aryl iodide and arylboronic acid in a simple and efficient way with moderate yield and stereoselectivity. MDPI 2015-08-03 /pmc/articles/PMC6331821/ /pubmed/26247925 http://dx.doi.org/10.3390/molecules200814022 Text en © 2015 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 license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Lee, Dahye
Park, Sunhwa
Yu, Yoseb
Shin, Kye Jung
Seo, Jae Hong
Palladium-Catalyzed One-Pot Approach to 3-(Diarylmethylene)oxindoles from Propiolamidoaryl Triflate
title Palladium-Catalyzed One-Pot Approach to 3-(Diarylmethylene)oxindoles from Propiolamidoaryl Triflate
title_full Palladium-Catalyzed One-Pot Approach to 3-(Diarylmethylene)oxindoles from Propiolamidoaryl Triflate
title_fullStr Palladium-Catalyzed One-Pot Approach to 3-(Diarylmethylene)oxindoles from Propiolamidoaryl Triflate
title_full_unstemmed Palladium-Catalyzed One-Pot Approach to 3-(Diarylmethylene)oxindoles from Propiolamidoaryl Triflate
title_short Palladium-Catalyzed One-Pot Approach to 3-(Diarylmethylene)oxindoles from Propiolamidoaryl Triflate
title_sort palladium-catalyzed one-pot approach to 3-(diarylmethylene)oxindoles from propiolamidoaryl triflate
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6331821/
https://www.ncbi.nlm.nih.gov/pubmed/26247925
http://dx.doi.org/10.3390/molecules200814022
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