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Volumn 75, Issue 23, 2010, Pages 8283-8286

Bidentate P, N-P ligand for nickel-catalyzed cross-coupling of aryl or benzyl chlorides with ArMgX

Author keywords

[No Author keywords available]

Indexed keywords

BENZYL CHLORIDES; BIDENTATE LIGANDS; CROSS COUPLING REACTIONS; CROSS-COUPLINGS; EQUIMOLAR AMOUNT; IN-SITU; P LIGANDS; PHOSPHINE COMPLEX; ROOM TEMPERATURE; SINGLE CRYSTAL X-RAY DIFFRACTION; STABLE COMPLEXES;

EID: 78650297372     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo1016458     Document Type: Article
Times cited : (45)

References (86)
  • 83
    • 78650256589 scopus 로고    scopus 로고
    • Part of the reagent is used up in the reduction of Ni(II) to Ni(0), and operation of Schlenck equilibrium to further reduce active ArMgX also cannot be ruled out; for previous examples of using 2 equiv of reagent, see refs 8h and 16b
    • Part of the reagent is used up in the reduction of Ni(II) to Ni(0), and operation of Schlenck equilibrium to further reduce active ArMgX also cannot be ruled out; for previous examples of using 2 equiv of reagent, see refs 8h and 16b.
  • 86
    • 78650276327 scopus 로고    scopus 로고
    • We observed that with allyl chloride the coupling product can be obtained in high yield without any catalyst. Hence, such examples were not included in this revision. We thank a reviewer for bringing this issue to our attention
    • We observed that with allyl chloride the coupling product can be obtained in high yield without any catalyst. Hence, such examples were not included in this revision. We thank a reviewer for bringing this issue to our attention.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.