An aza-Diels–Alder approach to chlorinated quinolines, benzoquinolines, and polybenzoquinolines

Quinolines and quinoline-containing macromolecules are renowned for their valuable biological activities and excellent materials properties. Herein, we validate a general strategy for the synthesis of chloro-containing quinoline, benzoquinoline and polybenzoquinoline variants via the aza-Diels–Alder...

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Autores principales: Kim, Juhwan, Umerani, Mehran J., Kurakake, Reina, Qin, Huiting, Ziller, Joseph W., Gorodetsky, Alon A., Park, Young S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Chemistry
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8697586/
https://www.ncbi.nlm.nih.gov/pubmed/35423954
http://dx.doi.org/10.1039/d0ra06744j
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author Kim, Juhwan
Umerani, Mehran J.
Kurakake, Reina
Qin, Huiting
Ziller, Joseph W.
Gorodetsky, Alon A.
Park, Young S.
author_facet Kim, Juhwan
Umerani, Mehran J.
Kurakake, Reina
Qin, Huiting
Ziller, Joseph W.
Gorodetsky, Alon A.
Park, Young S.
author_sort Kim, Juhwan
collection PubMed
description Quinolines and quinoline-containing macromolecules are renowned for their valuable biological activities and excellent materials properties. Herein, we validate a general strategy for the synthesis of chloro-containing quinoline, benzoquinoline and polybenzoquinoline variants via the aza-Diels–Alder reaction. The described findings could be ultimately implemented in other synthetic pathways and may open new opportunities for analogous quinoline-derived materials.
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spelling pubmed-86975862022-04-13 An aza-Diels–Alder approach to chlorinated quinolines, benzoquinolines, and polybenzoquinolines Kim, Juhwan Umerani, Mehran J. Kurakake, Reina Qin, Huiting Ziller, Joseph W. Gorodetsky, Alon A. Park, Young S. RSC Adv Chemistry Quinolines and quinoline-containing macromolecules are renowned for their valuable biological activities and excellent materials properties. Herein, we validate a general strategy for the synthesis of chloro-containing quinoline, benzoquinoline and polybenzoquinoline variants via the aza-Diels–Alder reaction. The described findings could be ultimately implemented in other synthetic pathways and may open new opportunities for analogous quinoline-derived materials. The Royal Society of Chemistry 2021-04-14 /pmc/articles/PMC8697586/ /pubmed/35423954 http://dx.doi.org/10.1039/d0ra06744j Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Kim, Juhwan
Umerani, Mehran J.
Kurakake, Reina
Qin, Huiting
Ziller, Joseph W.
Gorodetsky, Alon A.
Park, Young S.
An aza-Diels–Alder approach to chlorinated quinolines, benzoquinolines, and polybenzoquinolines
title An aza-Diels–Alder approach to chlorinated quinolines, benzoquinolines, and polybenzoquinolines
title_full An aza-Diels–Alder approach to chlorinated quinolines, benzoquinolines, and polybenzoquinolines
title_fullStr An aza-Diels–Alder approach to chlorinated quinolines, benzoquinolines, and polybenzoquinolines
title_full_unstemmed An aza-Diels–Alder approach to chlorinated quinolines, benzoquinolines, and polybenzoquinolines
title_short An aza-Diels–Alder approach to chlorinated quinolines, benzoquinolines, and polybenzoquinolines
title_sort aza-diels–alder approach to chlorinated quinolines, benzoquinolines, and polybenzoquinolines
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8697586/
https://www.ncbi.nlm.nih.gov/pubmed/35423954
http://dx.doi.org/10.1039/d0ra06744j
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