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.

Bibliographic Details
Main Authors: Piotr Roszkowski, Jan. K. Maurin, Zbigniew Czarnocki
Format: Article
Language:English
Published: Beilstein-Institut 2015-08-01
Series:Beilstein Journal of Organic Chemistry
Subjects:
Online Access:https://doi.org/10.3762/bjoc.11.164
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spelling doaj-e5eb73ed00134ec6b866c4895865a7c82021-03-02T10:05:00ZengBeilstein-InstitutBeilstein Journal of Organic Chemistry1860-53972015-08-011111509151310.3762/bjoc.11.1641860-5397-11-164The enantioselective synthesis of (S)-(+)-mianserin and (S)-(+)-epinastinePiotr Roszkowski0Jan. K. Maurin1Zbigniew Czarnocki2Faculty of Chemistry, University of Warsaw, Pasteura 1, 02-093, Warsaw, PolandNational Medicines Institute, Chełmska 30/34, 00-725 Warsaw, Poland andFaculty of Chemistry, University of Warsaw, Pasteura 1, 02-093, Warsaw, PolandA 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.https://doi.org/10.3762/bjoc.11.164chiral diaminesenantioselective reductionepinastinemianserinruthenium complexes
collection DOAJ
language English
format Article
sources DOAJ
author Piotr Roszkowski
Jan. K. Maurin
Zbigniew Czarnocki
spellingShingle Piotr Roszkowski
Jan. K. Maurin
Zbigniew Czarnocki
The enantioselective synthesis of (S)-(+)-mianserin and (S)-(+)-epinastine
Beilstein Journal of Organic Chemistry
chiral diamines
enantioselective reduction
epinastine
mianserin
ruthenium complexes
author_facet Piotr Roszkowski
Jan. K. Maurin
Zbigniew Czarnocki
author_sort Piotr Roszkowski
title The enantioselective synthesis of (S)-(+)-mianserin and (S)-(+)-epinastine
title_short 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_sort enantioselective synthesis of (s)-(+)-mianserin and (s)-(+)-epinastine
publisher Beilstein-Institut
series Beilstein Journal of Organic Chemistry
issn 1860-5397
publishDate 2015-08-01
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.
topic chiral diamines
enantioselective reduction
epinastine
mianserin
ruthenium complexes
url https://doi.org/10.3762/bjoc.11.164
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