Co(III)-Catalyzed, Internal and Terminal Alkyne-Compatible Synthesis of Indoles

A Co­(III)-catalyzed, internal and terminal alkyne-compatible indole synthesis protocol is reported herein. The N-amino (hydrazine) group imparts distinct, diverse reactivity patterns for directed C–H functionalization/cyclization reactions. Notable synthetic features include regioselectivity for a...

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Veröffentlicht in:Organic letters 2016-08, Vol.18 (15), p.3806-3809
Hauptverfasser: Zhou, Shuguang, Wang, Jinhu, Wang, Lili, Chen, Kehao, Song, Chao, Zhu, Jin
Format: Artikel
Sprache:eng
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Zusammenfassung:A Co­(III)-catalyzed, internal and terminal alkyne-compatible indole synthesis protocol is reported herein. The N-amino (hydrazine) group imparts distinct, diverse reactivity patterns for directed C–H functionalization/cyclization reactions. Notable synthetic features include regioselectivity for a meta-substituted arylhydrazine, regioselectivity for a chain-branched terminal alkyne, formal incorporation of an acetylenic unit through C2-desilylation on a C2-silylated indole derivative, formal inversion of regioselectivity through consecutive C3-derivatization and C2-desilylation processes, and formal bond migration for a linear-chain terminal alkyne.
ISSN:1523-7060
1523-7052
DOI:10.1021/acs.orglett.6b01805