메뉴 건너뛰기




Volumn 49, Issue 32, 2010, Pages 5541-5544

Synthesis of polyarylated methanes through cross-coupling of tricarbonylchromium-activated benzyllithiums

Author keywords

C c coupling; Chromium organolithium; Palladium; Triarylmethanes

Indexed keywords

ARYL BROMIDES; BENZYLIC; C-C COUPLING; CHEMICAL EQUATIONS; CROSS COUPLING REACTIONS; CROSS-COUPLINGS; ORGANOLITHIUMS;

EID: 77955019939     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201000957     Document Type: Article
Times cited : (98)

References (35)
  • 14
    • 0001238582 scopus 로고    scopus 로고
    • For a complementary procedure involving vicarious nucleophilic substitution of nitroarenes see: A. R. Katritzky, D. Toader, J. Org. Chem. 1997, 62, 4137.
    • (1997) J. Org. Chem. , vol.62 , pp. 4137
    • Katritzky, A.R.1    Toader, D.2
  • 23
    • 34247624723 scopus 로고    scopus 로고
    • Ed.: L. E. Overman, Wiley, New York
    • M. Uemura in Organic Reactions, Vol. 67 (Ed.: L. E. Overman), Wiley, New York, 2006, p. 217.
    • (2006) Organic Reactions , vol.67 , pp. 217
    • Uemura, M.1
  • 29
    • 0003979828 scopus 로고    scopus 로고
    • Academic Press, San Diego
    • R. J. Sundberg, Indoles, Academic Press, San Diego, 1996.
    • (1996) Indoles
    • Sundberg, R.J.1
  • 30
    • 77955039509 scopus 로고    scopus 로고
    • 2, 1 exhibited approximately 50% deprotonation, whereas 3 was only 10% deprotonated.
    • 2, 1 exhibited approximately 50% deprotonation, whereas 3 was only 10% deprotonated.
  • 31
    • 77955024167 scopus 로고    scopus 로고
    • CCDC 775771 (1.0) and 765716 (27b) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
    • CCDC 775771 (1.0) and 765716 (27b) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data- request/cif
  • 34
    • 77955037801 scopus 로고    scopus 로고
    • Alternatively, the coordinated arene can be purified first and then simply decomplexed by exposure to light and air. A solution of coordinated arene 2 a exposed to light and air provided triphenylmethane in 98% isolated yield.
    • Alternatively, the coordinated arene can be purified first and then simply decomplexed by exposure to light and air. A solution of coordinated arene 2 a exposed to light and air provided triphenylmethane in 98% isolated yield.
  • 35
    • 0036643455 scopus 로고    scopus 로고
    • For cross-coupling reactions with organolithium reagents see : S.I. Murahashi, J. Organomet. Chem. 2002, 653, 27.
    • (2002) J. Organomet. Chem. , vol.653 , pp. 27
    • Murahashi, S.I.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.