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Asymmetric Brønsted acid-catalyzed aza-Diels–Alder reaction of cyclic C-acylimines with cyclopentadiene
A new chiral Brønsted acid-catalyzed aza-Diels–Alder reaction of cyclic C-acylimines with cyclopentadiene has been developed. The reaction provides optically active aza-tetracycles in good yields with high diastereo- and enantioselectivities under mild reaction conditions.
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3511017/ https://www.ncbi.nlm.nih.gov/pubmed/23209517 http://dx.doi.org/10.3762/bjoc.8.208 |
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author | Rueping, Magnus Raja, Sadiya |
author_facet | Rueping, Magnus Raja, Sadiya |
author_sort | Rueping, Magnus |
collection | PubMed |
description | A new chiral Brønsted acid-catalyzed aza-Diels–Alder reaction of cyclic C-acylimines with cyclopentadiene has been developed. The reaction provides optically active aza-tetracycles in good yields with high diastereo- and enantioselectivities under mild reaction conditions. |
format | Online Article Text |
id | pubmed-3511017 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-35110172012-12-03 Asymmetric Brønsted acid-catalyzed aza-Diels–Alder reaction of cyclic C-acylimines with cyclopentadiene Rueping, Magnus Raja, Sadiya Beilstein J Org Chem Full Research Paper A new chiral Brønsted acid-catalyzed aza-Diels–Alder reaction of cyclic C-acylimines with cyclopentadiene has been developed. The reaction provides optically active aza-tetracycles in good yields with high diastereo- and enantioselectivities under mild reaction conditions. Beilstein-Institut 2012-10-23 /pmc/articles/PMC3511017/ /pubmed/23209517 http://dx.doi.org/10.3762/bjoc.8.208 Text en Copyright © 2012, Rueping and Raja 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 Rueping, Magnus Raja, Sadiya Asymmetric Brønsted acid-catalyzed aza-Diels–Alder reaction of cyclic C-acylimines with cyclopentadiene |
title | Asymmetric Brønsted acid-catalyzed aza-Diels–Alder reaction of cyclic C-acylimines with cyclopentadiene |
title_full | Asymmetric Brønsted acid-catalyzed aza-Diels–Alder reaction of cyclic C-acylimines with cyclopentadiene |
title_fullStr | Asymmetric Brønsted acid-catalyzed aza-Diels–Alder reaction of cyclic C-acylimines with cyclopentadiene |
title_full_unstemmed | Asymmetric Brønsted acid-catalyzed aza-Diels–Alder reaction of cyclic C-acylimines with cyclopentadiene |
title_short | Asymmetric Brønsted acid-catalyzed aza-Diels–Alder reaction of cyclic C-acylimines with cyclopentadiene |
title_sort | asymmetric brønsted acid-catalyzed aza-diels–alder reaction of cyclic c-acylimines with cyclopentadiene |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3511017/ https://www.ncbi.nlm.nih.gov/pubmed/23209517 http://dx.doi.org/10.3762/bjoc.8.208 |
work_keys_str_mv | AT ruepingmagnus asymmetricbrønstedacidcatalyzedazadielsalderreactionofcycliccacylimineswithcyclopentadiene AT rajasadiya asymmetricbrønstedacidcatalyzedazadielsalderreactionofcycliccacylimineswithcyclopentadiene |