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Copper-Catalyzed Oxidative Homo- and Cross-Coupling of Grignard Reagents Using Diaziridinone
[Image: see text] Transition-metal-catalyzed cross-coupling reactions are among the most powerful synthetic transformations. This paper describes an efficient copper-catalyzed homo- and cross-coupling of Grignard reagents with di-tert-butyldiaziridinone as oxidant under mild conditions, giving the c...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4260645/ https://www.ncbi.nlm.nih.gov/pubmed/25420218 http://dx.doi.org/10.1021/ol5030103 |
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author | Zhu, Yingguang Xiong, Tao Han, Wenyong Shi, Yian |
author_facet | Zhu, Yingguang Xiong, Tao Han, Wenyong Shi, Yian |
author_sort | Zhu, Yingguang |
collection | PubMed |
description | [Image: see text] Transition-metal-catalyzed cross-coupling reactions are among the most powerful synthetic transformations. This paper describes an efficient copper-catalyzed homo- and cross-coupling of Grignard reagents with di-tert-butyldiaziridinone as oxidant under mild conditions, giving the coupling products in good to excellent yields. The reaction process has a broad substrate scope and is also effective for the C(sp)–C(sp(3)) coupling. |
format | Online Article Text |
id | pubmed-4260645 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-42606452015-11-24 Copper-Catalyzed Oxidative Homo- and Cross-Coupling of Grignard Reagents Using Diaziridinone Zhu, Yingguang Xiong, Tao Han, Wenyong Shi, Yian Org Lett [Image: see text] Transition-metal-catalyzed cross-coupling reactions are among the most powerful synthetic transformations. This paper describes an efficient copper-catalyzed homo- and cross-coupling of Grignard reagents with di-tert-butyldiaziridinone as oxidant under mild conditions, giving the coupling products in good to excellent yields. The reaction process has a broad substrate scope and is also effective for the C(sp)–C(sp(3)) coupling. American Chemical Society 2014-11-24 2014-12-05 /pmc/articles/PMC4260645/ /pubmed/25420218 http://dx.doi.org/10.1021/ol5030103 Text en Copyright © 2014 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Zhu, Yingguang Xiong, Tao Han, Wenyong Shi, Yian Copper-Catalyzed Oxidative Homo- and Cross-Coupling of Grignard Reagents Using Diaziridinone |
title | Copper-Catalyzed Oxidative Homo- and Cross-Coupling
of Grignard Reagents Using Diaziridinone |
title_full | Copper-Catalyzed Oxidative Homo- and Cross-Coupling
of Grignard Reagents Using Diaziridinone |
title_fullStr | Copper-Catalyzed Oxidative Homo- and Cross-Coupling
of Grignard Reagents Using Diaziridinone |
title_full_unstemmed | Copper-Catalyzed Oxidative Homo- and Cross-Coupling
of Grignard Reagents Using Diaziridinone |
title_short | Copper-Catalyzed Oxidative Homo- and Cross-Coupling
of Grignard Reagents Using Diaziridinone |
title_sort | copper-catalyzed oxidative homo- and cross-coupling
of grignard reagents using diaziridinone |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4260645/ https://www.ncbi.nlm.nih.gov/pubmed/25420218 http://dx.doi.org/10.1021/ol5030103 |
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