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BINOL as a chiral element in mechanically interlocked molecules

In this minireview we present the use of the axially chiral 1,1'-binaphthyl-2,2'-diol (BINOL) unit as a stereogenic element in mechanically interlocked molecules (MIMs). We describe the synthesis and properties of such BINOL-based chiral MIMs, together with their use in further diastereose...

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Autores principales: Krajnc, Matthias, Niemeyer, Jochen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9086503/
https://www.ncbi.nlm.nih.gov/pubmed/35601990
http://dx.doi.org/10.3762/bjoc.18.53
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author Krajnc, Matthias
Niemeyer, Jochen
author_facet Krajnc, Matthias
Niemeyer, Jochen
author_sort Krajnc, Matthias
collection PubMed
description In this minireview we present the use of the axially chiral 1,1'-binaphthyl-2,2'-diol (BINOL) unit as a stereogenic element in mechanically interlocked molecules (MIMs). We describe the synthesis and properties of such BINOL-based chiral MIMs, together with their use in further diastereoselective modifications, their application in asymmetric catalysis, and their use in stereoselective chemosensing. Given the growing importance of mechanically interlocked molecules and the key advantages of the privileged chiral BINOL backbone, we believe that this research area will continue to grow and deliver many useful applications in the future.
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spelling pubmed-90865032022-05-19 BINOL as a chiral element in mechanically interlocked molecules Krajnc, Matthias Niemeyer, Jochen Beilstein J Org Chem Review In this minireview we present the use of the axially chiral 1,1'-binaphthyl-2,2'-diol (BINOL) unit as a stereogenic element in mechanically interlocked molecules (MIMs). We describe the synthesis and properties of such BINOL-based chiral MIMs, together with their use in further diastereoselective modifications, their application in asymmetric catalysis, and their use in stereoselective chemosensing. Given the growing importance of mechanically interlocked molecules and the key advantages of the privileged chiral BINOL backbone, we believe that this research area will continue to grow and deliver many useful applications in the future. Beilstein-Institut 2022-05-06 /pmc/articles/PMC9086503/ /pubmed/35601990 http://dx.doi.org/10.3762/bjoc.18.53 Text en Copyright © 2022, Krajnc and Niemeyer https://creativecommons.org/licenses/by/4.0/This is an open access article licensed under the terms of the Beilstein-Institut Open Access License Agreement (https://www.beilstein-journals.org/bjoc/terms/terms), which is identical to the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/) ). The reuse of material under this license requires that the author(s), source and license are credited. Third-party material in this article could be subject to other licenses (typically indicated in the credit line), and in this case, users are required to obtain permission from the license holder to reuse the material.
spellingShingle Review
Krajnc, Matthias
Niemeyer, Jochen
BINOL as a chiral element in mechanically interlocked molecules
title BINOL as a chiral element in mechanically interlocked molecules
title_full BINOL as a chiral element in mechanically interlocked molecules
title_fullStr BINOL as a chiral element in mechanically interlocked molecules
title_full_unstemmed BINOL as a chiral element in mechanically interlocked molecules
title_short BINOL as a chiral element in mechanically interlocked molecules
title_sort binol as a chiral element in mechanically interlocked molecules
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9086503/
https://www.ncbi.nlm.nih.gov/pubmed/35601990
http://dx.doi.org/10.3762/bjoc.18.53
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