Synthesis of 2,3-Disubstituted NH Indoles via Rhodium(III)-Catalyzed C-H Activation of Arylnitrones and Coupling with Diazo Compounds
A rhodium-catalyzed intermolecular coupling between arylnitrones and diazo compounds by C-H activation/[4 + 1] annulation with a C(N2)-C(acyl) bond cleavage is reported, and 2,3-disubstituted NH indoles are directly synthesized in up to a 94% yield. A variety of functional groups are applicable to this reaction to give the corresponding products with high selectivity. Compared to other previously reported Rh(III)-catalyzed synthesis of homologous series, this method is simpler, more general, and more efficient.
Medienart: |
E-Artikel |
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Erscheinungsjahr: |
2017 |
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Erschienen: |
2017 |
Enthalten in: |
Zur Gesamtaufnahme - volume:82 |
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Enthalten in: |
The Journal of organic chemistry - 82(2017), 21 vom: 03. Nov., Seite 11505-11511 |
Sprache: |
Englisch |
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Beteiligte Personen: |
Guo, Xin [VerfasserIn] |
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Links: |
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Themen: |
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Anmerkungen: |
Date Completed 28.05.2018 Date Revised 28.05.2018 published: Print-Electronic Citation Status PubMed-not-MEDLINE |
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doi: |
10.1021/acs.joc.7b02105 |
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funding: |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
NLM275935256 |
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520 | |a A rhodium-catalyzed intermolecular coupling between arylnitrones and diazo compounds by C-H activation/[4 + 1] annulation with a C(N2)-C(acyl) bond cleavage is reported, and 2,3-disubstituted NH indoles are directly synthesized in up to a 94% yield. A variety of functional groups are applicable to this reaction to give the corresponding products with high selectivity. Compared to other previously reported Rh(III)-catalyzed synthesis of homologous series, this method is simpler, more general, and more efficient | ||
650 | 4 | |a Journal Article | |
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700 | 1 | |a Han, Jianwei |e verfasserin |4 aut | |
700 | 1 | |a Liu, Yafeng |e verfasserin |4 aut | |
700 | 1 | |a Qin, Mingda |e verfasserin |4 aut | |
700 | 1 | |a Zhang, Xueguo |e verfasserin |4 aut | |
700 | 1 | |a Chen, Baohua |e verfasserin |4 aut | |
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