One-pot tandem cyclization of enantiopure asymmetric cis-2,5-disubstituted pyrrolidines: Facile access to chiral 10-heteroazatriquinanes

A series of chiral 10-heteroazatriquinanes were synthesized from enantiopure asymmetric cis-2,5-disubstituted pyrrolidines through a one-pot tandem cyclization procedure. The structures and configurations of these new chiral 10-heteroazatriquinanes are confirmed by X-ray single-crystal diffraction a...

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Autores principales: Wang, Ping-An, Zhang, Sheng-Yong, Kagan, Henri B
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/PMC3596118/
https://www.ncbi.nlm.nih.gov/pubmed/23503199
http://dx.doi.org/10.3762/bjoc.9.32
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author Wang, Ping-An
Zhang, Sheng-Yong
Kagan, Henri B
author_facet Wang, Ping-An
Zhang, Sheng-Yong
Kagan, Henri B
author_sort Wang, Ping-An
collection PubMed
description A series of chiral 10-heteroazatriquinanes were synthesized from enantiopure asymmetric cis-2,5-disubstituted pyrrolidines through a one-pot tandem cyclization procedure. The structures and configurations of these new chiral 10-heteroazatriquinanes are confirmed by X-ray single-crystal diffraction analysis.
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spelling pubmed-35961182013-03-15 One-pot tandem cyclization of enantiopure asymmetric cis-2,5-disubstituted pyrrolidines: Facile access to chiral 10-heteroazatriquinanes Wang, Ping-An Zhang, Sheng-Yong Kagan, Henri B Beilstein J Org Chem Full Research Paper A series of chiral 10-heteroazatriquinanes were synthesized from enantiopure asymmetric cis-2,5-disubstituted pyrrolidines through a one-pot tandem cyclization procedure. The structures and configurations of these new chiral 10-heteroazatriquinanes are confirmed by X-ray single-crystal diffraction analysis. Beilstein-Institut 2013-02-07 /pmc/articles/PMC3596118/ /pubmed/23503199 http://dx.doi.org/10.3762/bjoc.9.32 Text en Copyright © 2013, Wang 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
Wang, Ping-An
Zhang, Sheng-Yong
Kagan, Henri B
One-pot tandem cyclization of enantiopure asymmetric cis-2,5-disubstituted pyrrolidines: Facile access to chiral 10-heteroazatriquinanes
title One-pot tandem cyclization of enantiopure asymmetric cis-2,5-disubstituted pyrrolidines: Facile access to chiral 10-heteroazatriquinanes
title_full One-pot tandem cyclization of enantiopure asymmetric cis-2,5-disubstituted pyrrolidines: Facile access to chiral 10-heteroazatriquinanes
title_fullStr One-pot tandem cyclization of enantiopure asymmetric cis-2,5-disubstituted pyrrolidines: Facile access to chiral 10-heteroazatriquinanes
title_full_unstemmed One-pot tandem cyclization of enantiopure asymmetric cis-2,5-disubstituted pyrrolidines: Facile access to chiral 10-heteroazatriquinanes
title_short One-pot tandem cyclization of enantiopure asymmetric cis-2,5-disubstituted pyrrolidines: Facile access to chiral 10-heteroazatriquinanes
title_sort one-pot tandem cyclization of enantiopure asymmetric cis-2,5-disubstituted pyrrolidines: facile access to chiral 10-heteroazatriquinanes
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3596118/
https://www.ncbi.nlm.nih.gov/pubmed/23503199
http://dx.doi.org/10.3762/bjoc.9.32
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