Nickel-catalyzed cross-electrophile coupling of aryl bromides and cyclic secondary alkyl bromides with spiro-bidentate-pyox ligands

The cross-electrophile coupling of aryl bromides and cyclic secondary alkyl bromides catalyzed by nickel/spiro-bidentate-pyox ligands with lithium chloride as the additive for the Csp 2 -Csp 3 bond formation was reported. The reaction could tolerate functional groups such as sulfonamide, ester, alde...

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Veröffentlicht in:New journal of chemistry 2021-09, Vol.45 (36), p.16477-16481
Hauptverfasser: Gao, Nanxing, Li, Yanshun, Cao, Guorui, Teng, Dawei
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Sprache:eng
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Zusammenfassung:The cross-electrophile coupling of aryl bromides and cyclic secondary alkyl bromides catalyzed by nickel/spiro-bidentate-pyox ligands with lithium chloride as the additive for the Csp 2 -Csp 3 bond formation was reported. The reaction could tolerate functional groups such as sulfonamide, ester, aldehyde, ketone, protected indolyl, tert-butoxycarbonyl, aryl nitriles and aryl chloride. Various aryl-cyclic secondary alkyl Csp 2 -Csp 3 bond products were synthesized under optimal reaction conditions (19 examples). The cross-electrophile coupling catalyzed by nickel/spiro-bidentate-pyox ligands with lithium chloride as the additive was reported, which has good functional group tolerance (19 examples).
ISSN:1144-0546
1369-9261
DOI:10.1039/d1nj02677a