Enantioselective preparation of mechanically planar chiral rotaxanes by kinetic resolution strategy

Since the discovery of mechanically planar chiral rotaxanes and topologically chiral catenanes, their asymmetric synthesis has been a long-standing challenge. Here, the authors report enantioselective preparation of mechanically planar chiral rotaxanes with up to 99.9% ee in 29% yield.

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Main Authors: Ayumi Imayoshi, Bhatraju Vasantha Lakshmi, Yoshihiro Ueda, Tomoyuki Yoshimura, Aki Matayoshi, Takumi Furuta, Takeo Kawabata
Format: article
Language:EN
Published: Nature Portfolio 2021
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Online Access:https://doaj.org/article/e8236e10a064472da76bf6e8c01ff2d3
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spelling oai:doaj.org-article:e8236e10a064472da76bf6e8c01ff2d32021-12-02T14:01:14ZEnantioselective preparation of mechanically planar chiral rotaxanes by kinetic resolution strategy10.1038/s41467-020-20372-02041-1723https://doaj.org/article/e8236e10a064472da76bf6e8c01ff2d32021-01-01T00:00:00Zhttps://doi.org/10.1038/s41467-020-20372-0https://doaj.org/toc/2041-1723Since the discovery of mechanically planar chiral rotaxanes and topologically chiral catenanes, their asymmetric synthesis has been a long-standing challenge. Here, the authors report enantioselective preparation of mechanically planar chiral rotaxanes with up to 99.9% ee in 29% yield.Ayumi ImayoshiBhatraju Vasantha LakshmiYoshihiro UedaTomoyuki YoshimuraAki MatayoshiTakumi FurutaTakeo KawabataNature PortfolioarticleScienceQENNature Communications, Vol 12, Iss 1, Pp 1-7 (2021)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Ayumi Imayoshi
Bhatraju Vasantha Lakshmi
Yoshihiro Ueda
Tomoyuki Yoshimura
Aki Matayoshi
Takumi Furuta
Takeo Kawabata
Enantioselective preparation of mechanically planar chiral rotaxanes by kinetic resolution strategy
description Since the discovery of mechanically planar chiral rotaxanes and topologically chiral catenanes, their asymmetric synthesis has been a long-standing challenge. Here, the authors report enantioselective preparation of mechanically planar chiral rotaxanes with up to 99.9% ee in 29% yield.
format article
author Ayumi Imayoshi
Bhatraju Vasantha Lakshmi
Yoshihiro Ueda
Tomoyuki Yoshimura
Aki Matayoshi
Takumi Furuta
Takeo Kawabata
author_facet Ayumi Imayoshi
Bhatraju Vasantha Lakshmi
Yoshihiro Ueda
Tomoyuki Yoshimura
Aki Matayoshi
Takumi Furuta
Takeo Kawabata
author_sort Ayumi Imayoshi
title Enantioselective preparation of mechanically planar chiral rotaxanes by kinetic resolution strategy
title_short Enantioselective preparation of mechanically planar chiral rotaxanes by kinetic resolution strategy
title_full Enantioselective preparation of mechanically planar chiral rotaxanes by kinetic resolution strategy
title_fullStr Enantioselective preparation of mechanically planar chiral rotaxanes by kinetic resolution strategy
title_full_unstemmed Enantioselective preparation of mechanically planar chiral rotaxanes by kinetic resolution strategy
title_sort enantioselective preparation of mechanically planar chiral rotaxanes by kinetic resolution strategy
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/e8236e10a064472da76bf6e8c01ff2d3
work_keys_str_mv AT ayumiimayoshi enantioselectivepreparationofmechanicallyplanarchiralrotaxanesbykineticresolutionstrategy
AT bhatrajuvasanthalakshmi enantioselectivepreparationofmechanicallyplanarchiralrotaxanesbykineticresolutionstrategy
AT yoshihiroueda enantioselectivepreparationofmechanicallyplanarchiralrotaxanesbykineticresolutionstrategy
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AT akimatayoshi enantioselectivepreparationofmechanicallyplanarchiralrotaxanesbykineticresolutionstrategy
AT takumifuruta enantioselectivepreparationofmechanicallyplanarchiralrotaxanesbykineticresolutionstrategy
AT takeokawabata enantioselectivepreparationofmechanicallyplanarchiralrotaxanesbykineticresolutionstrategy
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