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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2015
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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. |
format | Online Article Text |
id | pubmed-6331821 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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