Supramolecular construction of a cyclobutane ring system with four different substituents in the solid state

Preparation of cyclobutanes with four different substituents is rare and often arduous. Here a cocrystallisation strategy enables the intermolecular [2+2] cross-photoreaction of non-symmetrical stilbene derivatives to obtain chiral tetrasubstituted cyclobutanes with up to four different substituents...

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Autores principales: Michael A. Sinnwell, Ryan H. Groeneman, Benjamin J. Ingenthron, Changan Li, Leonard R. MacGillivray
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/a6ea5b35ee29422d87485a9e4518e741
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spelling oai:doaj.org-article:a6ea5b35ee29422d87485a9e4518e7412021-12-02T16:57:12ZSupramolecular construction of a cyclobutane ring system with four different substituents in the solid state10.1038/s42004-021-00493-32399-3669https://doaj.org/article/a6ea5b35ee29422d87485a9e4518e7412021-05-01T00:00:00Zhttps://doi.org/10.1038/s42004-021-00493-3https://doaj.org/toc/2399-3669Preparation of cyclobutanes with four different substituents is rare and often arduous. Here a cocrystallisation strategy enables the intermolecular [2+2] cross-photoreaction of non-symmetrical stilbene derivatives to obtain chiral tetrasubstituted cyclobutanes with up to four different substituents in quantitative yield.Michael A. SinnwellRyan H. GroenemanBenjamin J. IngenthronChangan LiLeonard R. MacGillivrayNature PortfolioarticleChemistryQD1-999ENCommunications Chemistry, Vol 4, Iss 1, Pp 1-7 (2021)
institution DOAJ
collection DOAJ
language EN
topic Chemistry
QD1-999
spellingShingle Chemistry
QD1-999
Michael A. Sinnwell
Ryan H. Groeneman
Benjamin J. Ingenthron
Changan Li
Leonard R. MacGillivray
Supramolecular construction of a cyclobutane ring system with four different substituents in the solid state
description Preparation of cyclobutanes with four different substituents is rare and often arduous. Here a cocrystallisation strategy enables the intermolecular [2+2] cross-photoreaction of non-symmetrical stilbene derivatives to obtain chiral tetrasubstituted cyclobutanes with up to four different substituents in quantitative yield.
format article
author Michael A. Sinnwell
Ryan H. Groeneman
Benjamin J. Ingenthron
Changan Li
Leonard R. MacGillivray
author_facet Michael A. Sinnwell
Ryan H. Groeneman
Benjamin J. Ingenthron
Changan Li
Leonard R. MacGillivray
author_sort Michael A. Sinnwell
title Supramolecular construction of a cyclobutane ring system with four different substituents in the solid state
title_short Supramolecular construction of a cyclobutane ring system with four different substituents in the solid state
title_full Supramolecular construction of a cyclobutane ring system with four different substituents in the solid state
title_fullStr Supramolecular construction of a cyclobutane ring system with four different substituents in the solid state
title_full_unstemmed Supramolecular construction of a cyclobutane ring system with four different substituents in the solid state
title_sort supramolecular construction of a cyclobutane ring system with four different substituents in the solid state
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/a6ea5b35ee29422d87485a9e4518e741
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AT benjaminjingenthron supramolecularconstructionofacyclobutaneringsystemwithfourdifferentsubstituentsinthesolidstate
AT changanli supramolecularconstructionofacyclobutaneringsystemwithfourdifferentsubstituentsinthesolidstate
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