Diels-Alder Reactions of 12-Hydroxy-9(10→20)-5aH-abeo-abieta-1(10),8(9),12(13)-triene-11,14-dione

12-Hydroxy-9(10→20)-5aH-abeo-abieta-1(10),8(9),12(13)-triene-11,14-dione (quinone 2) served as the dienophile in numerous intermolecular Diels-Alder reactions. These cycloadditions were conducted either thermally (including microwave heating) or with Lewis acid activation. While most dienes reacted...

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Detalles Bibliográficos
Autores principales: Majetich, George, Zhang, Yong, Tian, Xinrong, Zou, Ge, Li, Yang, Wang, Yangyang, Hu, Shougang, Huddleston, Eric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2013
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6269985/
https://www.ncbi.nlm.nih.gov/pubmed/23771059
http://dx.doi.org/10.3390/molecules18066969
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author Majetich, George
Zhang, Yong
Tian, Xinrong
Zou, Ge
Li, Yang
Wang, Yangyang
Hu, Shougang
Huddleston, Eric
author_facet Majetich, George
Zhang, Yong
Tian, Xinrong
Zou, Ge
Li, Yang
Wang, Yangyang
Hu, Shougang
Huddleston, Eric
author_sort Majetich, George
collection PubMed
description 12-Hydroxy-9(10→20)-5aH-abeo-abieta-1(10),8(9),12(13)-triene-11,14-dione (quinone 2) served as the dienophile in numerous intermolecular Diels-Alder reactions. These cycloadditions were conducted either thermally (including microwave heating) or with Lewis acid activation. While most dienes reacted with quinone 2 in good chemical yield, others were incompatible under the experimental conditions used.
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spelling pubmed-62699852018-12-17 Diels-Alder Reactions of 12-Hydroxy-9(10→20)-5aH-abeo-abieta-1(10),8(9),12(13)-triene-11,14-dione Majetich, George Zhang, Yong Tian, Xinrong Zou, Ge Li, Yang Wang, Yangyang Hu, Shougang Huddleston, Eric Molecules Review 12-Hydroxy-9(10→20)-5aH-abeo-abieta-1(10),8(9),12(13)-triene-11,14-dione (quinone 2) served as the dienophile in numerous intermolecular Diels-Alder reactions. These cycloadditions were conducted either thermally (including microwave heating) or with Lewis acid activation. While most dienes reacted with quinone 2 in good chemical yield, others were incompatible under the experimental conditions used. MDPI 2013-06-14 /pmc/articles/PMC6269985/ /pubmed/23771059 http://dx.doi.org/10.3390/molecules18066969 Text en © 2013 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 Review
Majetich, George
Zhang, Yong
Tian, Xinrong
Zou, Ge
Li, Yang
Wang, Yangyang
Hu, Shougang
Huddleston, Eric
Diels-Alder Reactions of 12-Hydroxy-9(10→20)-5aH-abeo-abieta-1(10),8(9),12(13)-triene-11,14-dione
title Diels-Alder Reactions of 12-Hydroxy-9(10→20)-5aH-abeo-abieta-1(10),8(9),12(13)-triene-11,14-dione
title_full Diels-Alder Reactions of 12-Hydroxy-9(10→20)-5aH-abeo-abieta-1(10),8(9),12(13)-triene-11,14-dione
title_fullStr Diels-Alder Reactions of 12-Hydroxy-9(10→20)-5aH-abeo-abieta-1(10),8(9),12(13)-triene-11,14-dione
title_full_unstemmed Diels-Alder Reactions of 12-Hydroxy-9(10→20)-5aH-abeo-abieta-1(10),8(9),12(13)-triene-11,14-dione
title_short Diels-Alder Reactions of 12-Hydroxy-9(10→20)-5aH-abeo-abieta-1(10),8(9),12(13)-triene-11,14-dione
title_sort diels-alder reactions of 12-hydroxy-9(10→20)-5ah-abeo-abieta-1(10),8(9),12(13)-triene-11,14-dione
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6269985/
https://www.ncbi.nlm.nih.gov/pubmed/23771059
http://dx.doi.org/10.3390/molecules18066969
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