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 |
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Hauptverfasser: | , , , |
Format: | Artikel |
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). |
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ISSN: | 1144-0546 1369-9261 |
DOI: | 10.1039/d1nj02677a |