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Volumn 76, Issue 9, 2011, Pages 3588-3593

Nickel-mediated decarbonylative cross-coupling of phthalimides with in situ generated diorganozinc reagents

Author keywords

[No Author keywords available]

Indexed keywords

ARYL BROMIDES; BENZAMIDES; CROSS-COUPLINGS; DIORGANOZINC REAGENTS; HETEROATOMS; HIGH YIELD; IN-SITU; PHTHALIMIDE;

EID: 79955554079     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo200347j     Document Type: Article
Times cited : (46)

References (39)
  • 4
    • 34247859312 scopus 로고    scopus 로고
    • references cited therein.
    • Baudoin, O. Angew. Chem., Int. Ed. 2007, 46, 1373 and references cited therein.
    • (2007) Angew. Chem., Int. Ed. , vol.46 , pp. 1373
    • Baudoin, O.1
  • 25
    • 79955552762 scopus 로고    scopus 로고
    • note
    • A similar transformation with carboxylic anhydrides, but with limited diorganozinc scope, has been described. See ref 18.
  • 26
    • 79955566216 scopus 로고    scopus 로고
    • note
    • A more comprehensive list of optimization efforts is included in the Supporting Information.
  • 27
    • 79955558890 scopus 로고    scopus 로고
    • note
    • The two isomeric products were obtained in a 1:1.2 ratio and identified as decarbonylative alkylation products by mass spectrometry. Conclusive identification of the structure of the isomers in the mixture was unsuccessful.
  • 34
    • 0007887728 scopus 로고
    • Ni-CO bond strengths have been estimated to be anywhere from 28.3 to 47.1 kcal/mol; see
    • Ni-CO bond strengths have been estimated to be anywhere from 28.3 to 47.1 kcal/mol; see: Sunderlin, L. S.; Wang, D.; Squires, R. R. J. Am. Chem. Soc. 1992, 114, 2788
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 2788
    • Sunderlin, L.S.1    Wang, D.2    Squires, R.R.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.