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A Convenient One-Pot Preparation of 2-Methyl-3-(phenylthio- methyl)quinolines from Morita-Baylis-Hillman Adducts and Their Oxidation to the Corresponding Sulfones
A convenient one-pot preparation of 2-methyl-3-(phenylthiomethyl)quinolines from Morita-Baylis-Hillman adducts via conjugate addition of thiols followed by reductive cyclization with Fe/AcOH was developed. The 2-methyl-3-(phenylthiomethyl)quinolines were transformed into 2-methyl-3-(phenylsulfonylme...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268867/ https://www.ncbi.nlm.nih.gov/pubmed/22555297 http://dx.doi.org/10.3390/molecules17055081 |
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author | Ramesh, Chintakunta Lei, Po-Min Kavala, Veerababurao Kuo, Chun-Wei Yao, Ching-Fa |
author_facet | Ramesh, Chintakunta Lei, Po-Min Kavala, Veerababurao Kuo, Chun-Wei Yao, Ching-Fa |
author_sort | Ramesh, Chintakunta |
collection | PubMed |
description | A convenient one-pot preparation of 2-methyl-3-(phenylthiomethyl)quinolines from Morita-Baylis-Hillman adducts via conjugate addition of thiols followed by reductive cyclization with Fe/AcOH was developed. The 2-methyl-3-(phenylthiomethyl)quinolines were transformed into 2-methyl-3-(phenylsulfonylmethyl)quinolines via m-CPBA-mediated oxidation. |
format | Online Article Text |
id | pubmed-6268867 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62688672018-12-20 A Convenient One-Pot Preparation of 2-Methyl-3-(phenylthio- methyl)quinolines from Morita-Baylis-Hillman Adducts and Their Oxidation to the Corresponding Sulfones Ramesh, Chintakunta Lei, Po-Min Kavala, Veerababurao Kuo, Chun-Wei Yao, Ching-Fa Molecules Article A convenient one-pot preparation of 2-methyl-3-(phenylthiomethyl)quinolines from Morita-Baylis-Hillman adducts via conjugate addition of thiols followed by reductive cyclization with Fe/AcOH was developed. The 2-methyl-3-(phenylthiomethyl)quinolines were transformed into 2-methyl-3-(phenylsulfonylmethyl)quinolines via m-CPBA-mediated oxidation. MDPI 2012-05-03 /pmc/articles/PMC6268867/ /pubmed/22555297 http://dx.doi.org/10.3390/molecules17055081 Text en © 2012 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Ramesh, Chintakunta Lei, Po-Min Kavala, Veerababurao Kuo, Chun-Wei Yao, Ching-Fa A Convenient One-Pot Preparation of 2-Methyl-3-(phenylthio- methyl)quinolines from Morita-Baylis-Hillman Adducts and Their Oxidation to the Corresponding Sulfones |
title | A Convenient One-Pot Preparation of 2-Methyl-3-(phenylthio- methyl)quinolines from Morita-Baylis-Hillman Adducts and Their Oxidation to the Corresponding Sulfones |
title_full | A Convenient One-Pot Preparation of 2-Methyl-3-(phenylthio- methyl)quinolines from Morita-Baylis-Hillman Adducts and Their Oxidation to the Corresponding Sulfones |
title_fullStr | A Convenient One-Pot Preparation of 2-Methyl-3-(phenylthio- methyl)quinolines from Morita-Baylis-Hillman Adducts and Their Oxidation to the Corresponding Sulfones |
title_full_unstemmed | A Convenient One-Pot Preparation of 2-Methyl-3-(phenylthio- methyl)quinolines from Morita-Baylis-Hillman Adducts and Their Oxidation to the Corresponding Sulfones |
title_short | A Convenient One-Pot Preparation of 2-Methyl-3-(phenylthio- methyl)quinolines from Morita-Baylis-Hillman Adducts and Their Oxidation to the Corresponding Sulfones |
title_sort | convenient one-pot preparation of 2-methyl-3-(phenylthio- methyl)quinolines from morita-baylis-hillman adducts and their oxidation to the corresponding sulfones |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268867/ https://www.ncbi.nlm.nih.gov/pubmed/22555297 http://dx.doi.org/10.3390/molecules17055081 |
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