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Volumn 76, Issue 18, 2011, Pages 7573-7576

Stereochemistry of transmetalation of alkylboranes in nickel-catalyzed alkyl-alkyl cross-coupling reactions

Author keywords

[No Author keywords available]

Indexed keywords

CONFIGURATIONALLY; CROSS COUPLING REACTIONS; NICKEL CATALYST; NMR ANALYSIS; SUZUKI CROSS COUPLING; TRANSMETALATION;

EID: 80052767454     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo201263r     Document Type: Article
Times cited : (21)

References (40)
  • 4
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    • For a recent example of alkyl-alkyl cross-coupling reactions in target-oriented synthesis, see
    • For a recent example of alkyl-alkyl cross-coupling reactions in target-oriented synthesis, see: Griggs, N. D.; Phillips, A. J. Org. Lett. 2008, 10, 4955-4957
    • (2008) Org. Lett. , vol.10 , pp. 4955-4957
    • Griggs, N.D.1    Phillips, A.J.2
  • 5
    • 72949108920 scopus 로고    scopus 로고
    • For a representative sample of recent advances in palladium-catalyzed alkyl-aryl cross-coupling reactions, see
    • For a representative sample of recent advances in palladium-catalyzed alkyl-aryl cross-coupling reactions, see: Molander, G. A.; Canturk, B. Angew. Chem., Int. Ed. 2009, 48, 9240-9261
    • (2009) Angew. Chem., Int. Ed. , vol.48 , pp. 9240-9261
    • Molander, G.A.1    Canturk, B.2
  • 30
    • 0034678588 scopus 로고    scopus 로고
    • Alkylzinc halides racemize slowly at room temperature
    • Alkylzinc halides racemize slowly at room temperature: Guijarro, A.; Rieke, R. D. Angew. Chem., Int. Ed. 2000, 39, 1475-1479
    • (2000) Angew. Chem., Int. Ed. , vol.39 , pp. 1475-1479
    • Guijarro, A.1    Rieke, R.D.2
  • 35
    • 33847805244 scopus 로고
    • Whitesides pioneered the use of deuterium labeling to study the stereochemistry of reactions of alkylmetal intermediates
    • Whitesides pioneered the use of deuterium labeling to study the stereochemistry of reactions of alkylmetal intermediates: Bock, P. L.; Boschetto, D. J.; Rasmussen, J. R.; Demers, J. P.; Whitesides, G. M. J. Am. Chem. Soc. 1974, 96, 2814-2825
    • (1974) J. Am. Chem. Soc. , vol.96 , pp. 2814-2825
    • Bock, P.L.1    Boschetto, D.J.2    Rasmussen, J.R.3    Demers, J.P.4    Whitesides, G.M.5
  • 36
    • 0007623379 scopus 로고
    • Hydroboration is a syn addition process
    • Hydroboration is a syn addition process: Kabalka, G. W.; Bowman, N. S. J. Org. Chem. 1973, 38, 1607-1608
    • (1973) J. Org. Chem. , vol.38 , pp. 1607-1608
    • Kabalka, G.W.1    Bowman, N.S.2
  • 37
    • 20044375298 scopus 로고
    • Reductive elimination at nickel catalysts occurs with retention of configuration
    • Reductive elimination at nickel catalysts occurs with retention of configuration: Bäckvall, J. E.; Andell, O. S. Organometallics 1986, 5, 2350-2355
    • (1986) Organometallics , vol.5 , pp. 2350-2355
    • Bäckvall, J.E.1    Andell, O.S.2
  • 40
    • 0024581185 scopus 로고
    • Prepared from 2-bromoethanol according to
    • Prepared from 2-bromoethanol according to: Vader, J.; Sengers, H.; de Groot, A. Tetrahedron 1989, 45, 2131-2142
    • (1989) Tetrahedron , vol.45 , pp. 2131-2142
    • Vader, J.1    Sengers, H.2    De Groot, A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.