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The enantioselective synthesis of (S)-(+)-mianserin and (S)-(+)-epinastine
A simple enantioselective synthetic procedure for the preparation of mianserin and epinastine in optically pure form is described. The key step in the synthetic pathway is the asymmetric reduction of the cyclic imine using asymmetric transfer hydrogenation conditions.
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Beilstein-Institut
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4578372/ https://www.ncbi.nlm.nih.gov/pubmed/26425208 http://dx.doi.org/10.3762/bjoc.11.164 |
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author | Roszkowski, Piotr Maurin, Jan K Czarnocki, Zbigniew |
author_facet | Roszkowski, Piotr Maurin, Jan K Czarnocki, Zbigniew |
author_sort | Roszkowski, Piotr |
collection | PubMed |
description | A simple enantioselective synthetic procedure for the preparation of mianserin and epinastine in optically pure form is described. The key step in the synthetic pathway is the asymmetric reduction of the cyclic imine using asymmetric transfer hydrogenation conditions. |
format | Online Article Text |
id | pubmed-4578372 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Beilstein-Institut |
record_format | MEDLINE/PubMed |
spelling | pubmed-45783722015-09-30 The enantioselective synthesis of (S)-(+)-mianserin and (S)-(+)-epinastine Roszkowski, Piotr Maurin, Jan K Czarnocki, Zbigniew Beilstein J Org Chem Full Research Paper A simple enantioselective synthetic procedure for the preparation of mianserin and epinastine in optically pure form is described. The key step in the synthetic pathway is the asymmetric reduction of the cyclic imine using asymmetric transfer hydrogenation conditions. Beilstein-Institut 2015-08-28 /pmc/articles/PMC4578372/ /pubmed/26425208 http://dx.doi.org/10.3762/bjoc.11.164 Text en Copyright © 2015, Roszkowski 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 Roszkowski, Piotr Maurin, Jan K Czarnocki, Zbigniew The enantioselective synthesis of (S)-(+)-mianserin and (S)-(+)-epinastine |
title | The enantioselective synthesis of (S)-(+)-mianserin and (S)-(+)-epinastine |
title_full | The enantioselective synthesis of (S)-(+)-mianserin and (S)-(+)-epinastine |
title_fullStr | The enantioselective synthesis of (S)-(+)-mianserin and (S)-(+)-epinastine |
title_full_unstemmed | The enantioselective synthesis of (S)-(+)-mianserin and (S)-(+)-epinastine |
title_short | The enantioselective synthesis of (S)-(+)-mianserin and (S)-(+)-epinastine |
title_sort | enantioselective synthesis of (s)-(+)-mianserin and (s)-(+)-epinastine |
topic | Full Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4578372/ https://www.ncbi.nlm.nih.gov/pubmed/26425208 http://dx.doi.org/10.3762/bjoc.11.164 |
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