AgOTf-catalyzed one-pot reactions of 2-alkynylbenzaldoximes with α,β-unsaturated carbonyl compounds

AgOTf-catalyzed one-pot reactions of 2-alkynylbenzaldoximes with various α,β-unsaturated carbonyl compounds under mild conditions are described, which provides a facile and efficient pathway for the synthesis of 1-alkylated isoquinoline derivatives. The method tolerates a wide range of substrates an...

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Detalles Bibliográficos
Autores principales: Ding, Qiuping, Wang, Dan, Luo, Puying, Liu, Meiling, Pu, Shouzhi, Zhou, Liyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2013
Materias:
Full Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3817556/
https://www.ncbi.nlm.nih.gov/pubmed/24204406
http://dx.doi.org/10.3762/bjoc.9.231
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author Ding, Qiuping
Wang, Dan
Luo, Puying
Liu, Meiling
Pu, Shouzhi
Zhou, Liyun
author_facet Ding, Qiuping
Wang, Dan
Luo, Puying
Liu, Meiling
Pu, Shouzhi
Zhou, Liyun
author_sort Ding, Qiuping
collection PubMed
description AgOTf-catalyzed one-pot reactions of 2-alkynylbenzaldoximes with various α,β-unsaturated carbonyl compounds under mild conditions are described, which provides a facile and efficient pathway for the synthesis of 1-alkylated isoquinoline derivatives. The method tolerates a wide range of substrates and allows for the preparation of the products of interest in moderate to excellent yields.
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spelling pubmed-38175562013-11-07 AgOTf-catalyzed one-pot reactions of 2-alkynylbenzaldoximes with α,β-unsaturated carbonyl compounds Ding, Qiuping Wang, Dan Luo, Puying Liu, Meiling Pu, Shouzhi Zhou, Liyun Beilstein J Org Chem Full Research Paper AgOTf-catalyzed one-pot reactions of 2-alkynylbenzaldoximes with various α,β-unsaturated carbonyl compounds under mild conditions are described, which provides a facile and efficient pathway for the synthesis of 1-alkylated isoquinoline derivatives. The method tolerates a wide range of substrates and allows for the preparation of the products of interest in moderate to excellent yields. Beilstein-Institut 2013-09-27 /pmc/articles/PMC3817556/ /pubmed/24204406 http://dx.doi.org/10.3762/bjoc.9.231 Text en Copyright © 2013, Ding et al. https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Full Research Paper
Ding, Qiuping
Wang, Dan
Luo, Puying
Liu, Meiling
Pu, Shouzhi
Zhou, Liyun
AgOTf-catalyzed one-pot reactions of 2-alkynylbenzaldoximes with α,β-unsaturated carbonyl compounds
title AgOTf-catalyzed one-pot reactions of 2-alkynylbenzaldoximes with α,β-unsaturated carbonyl compounds
title_full AgOTf-catalyzed one-pot reactions of 2-alkynylbenzaldoximes with α,β-unsaturated carbonyl compounds
title_fullStr AgOTf-catalyzed one-pot reactions of 2-alkynylbenzaldoximes with α,β-unsaturated carbonyl compounds
title_full_unstemmed AgOTf-catalyzed one-pot reactions of 2-alkynylbenzaldoximes with α,β-unsaturated carbonyl compounds
title_short AgOTf-catalyzed one-pot reactions of 2-alkynylbenzaldoximes with α,β-unsaturated carbonyl compounds
title_sort agotf-catalyzed one-pot reactions of 2-alkynylbenzaldoximes with α,β-unsaturated carbonyl compounds
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3817556/
https://www.ncbi.nlm.nih.gov/pubmed/24204406
http://dx.doi.org/10.3762/bjoc.9.231
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