Construction of poly-N-heterocyclic scaffolds via the controlled reactivity of Cu-allenylidene intermediates

Copper-catalysed annulation of allenylidenes provides an opportunity to target the alpha, beta, or gamma positions of the allenylidene, but achieving this control is challenging. Here substrate control allows selectivity between these three positions in the enantioselective cyclisation of ethynyl be...

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Autores principales: Malla Reddy Gannarapu, Takanori Imai, Kentaro Iwaki, Seiji Tsuzuki, Norio Shibata
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/00fcb24ec6394783853319da33a9ebed
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spelling oai:doaj.org-article:00fcb24ec6394783853319da33a9ebed2021-11-21T12:03:53ZConstruction of poly-N-heterocyclic scaffolds via the controlled reactivity of Cu-allenylidene intermediates10.1038/s42004-021-00596-x2399-3669https://doaj.org/article/00fcb24ec6394783853319da33a9ebed2021-11-01T00:00:00Zhttps://doi.org/10.1038/s42004-021-00596-xhttps://doaj.org/toc/2399-3669Copper-catalysed annulation of allenylidenes provides an opportunity to target the alpha, beta, or gamma positions of the allenylidene, but achieving this control is challenging. Here substrate control allows selectivity between these three positions in the enantioselective cyclisation of ethynyl benzoxazinanones and sulfamate-derived cyclic imines.Malla Reddy GannarapuTakanori ImaiKentaro IwakiSeiji TsuzukiNorio ShibataNature PortfolioarticleChemistryQD1-999ENCommunications Chemistry, Vol 4, Iss 1, Pp 1-14 (2021)
institution DOAJ
collection DOAJ
language EN
topic Chemistry
QD1-999
spellingShingle Chemistry
QD1-999
Malla Reddy Gannarapu
Takanori Imai
Kentaro Iwaki
Seiji Tsuzuki
Norio Shibata
Construction of poly-N-heterocyclic scaffolds via the controlled reactivity of Cu-allenylidene intermediates
description Copper-catalysed annulation of allenylidenes provides an opportunity to target the alpha, beta, or gamma positions of the allenylidene, but achieving this control is challenging. Here substrate control allows selectivity between these three positions in the enantioselective cyclisation of ethynyl benzoxazinanones and sulfamate-derived cyclic imines.
format article
author Malla Reddy Gannarapu
Takanori Imai
Kentaro Iwaki
Seiji Tsuzuki
Norio Shibata
author_facet Malla Reddy Gannarapu
Takanori Imai
Kentaro Iwaki
Seiji Tsuzuki
Norio Shibata
author_sort Malla Reddy Gannarapu
title Construction of poly-N-heterocyclic scaffolds via the controlled reactivity of Cu-allenylidene intermediates
title_short Construction of poly-N-heterocyclic scaffolds via the controlled reactivity of Cu-allenylidene intermediates
title_full Construction of poly-N-heterocyclic scaffolds via the controlled reactivity of Cu-allenylidene intermediates
title_fullStr Construction of poly-N-heterocyclic scaffolds via the controlled reactivity of Cu-allenylidene intermediates
title_full_unstemmed Construction of poly-N-heterocyclic scaffolds via the controlled reactivity of Cu-allenylidene intermediates
title_sort construction of poly-n-heterocyclic scaffolds via the controlled reactivity of cu-allenylidene intermediates
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/00fcb24ec6394783853319da33a9ebed
work_keys_str_mv AT mallareddygannarapu constructionofpolynheterocyclicscaffoldsviathecontrolledreactivityofcuallenylideneintermediates
AT takanoriimai constructionofpolynheterocyclicscaffoldsviathecontrolledreactivityofcuallenylideneintermediates
AT kentaroiwaki constructionofpolynheterocyclicscaffoldsviathecontrolledreactivityofcuallenylideneintermediates
AT seijitsuzuki constructionofpolynheterocyclicscaffoldsviathecontrolledreactivityofcuallenylideneintermediates
AT norioshibata constructionofpolynheterocyclicscaffoldsviathecontrolledreactivityofcuallenylideneintermediates
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