메뉴 건너뛰기




Volumn 349, Issue 4-5, 2007, Pages 513-516

Asymmetric 1,4-addition of organoboron reagents to quinone monoketals catalyzed by a chiral diene/rhodium complex: A new synthetic route to enantioenriched 2-aryltetralones

Author keywords

Asymmetric catalysis; Boron; Chiral diene ligands; Conjugate addition; Quinone monoketals; Rhodium

Indexed keywords


EID: 34547163506     PISSN: 16154150     EISSN: 15213897     Source Type: Journal    
DOI: 10.1002/adsc.200600632     Document Type: Article
Times cited : (58)

References (58)
  • 3
    • 24644484333 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 5516.
    • (2005) Chem. Int. Ed , vol.44 , pp. 5516
    • Angew1
  • 6
    • 0037051609 scopus 로고    scopus 로고
    • nickel-catalyzed reaction: c D. J. Spielvogel, S. L. Buchwald, J. Am. Chem. Soc. 2002, 124, 3500.
    • nickel-catalyzed reaction: c) D. J. Spielvogel, S. L. Buchwald, J. Am. Chem. Soc. 2002, 124, 3500.
  • 11
  • 12
    • 0000530876 scopus 로고    scopus 로고
    • d) C. Fehr, Angew. Chem. 1996, 108, 2726;
    • (1996) Angew. Chem , vol.108 , pp. 2726
    • Fehr, C.1
  • 14
    • 0000184712 scopus 로고    scopus 로고
    • Ill, Eds, E. N. Jacobsen, A. Pfaltz, H. Yamamoto, Springer, Heidelberg
    • e) A. Yanagisawa, H. Yamamoto, in: Comprehensive Asymmetric Catalysis, Vol. Ill, (Eds.: E. N. Jacobsen, A. Pfaltz, H. Yamamoto), Springer, Heidelberg, 1999, p 1295;
    • (1999) Comprehensive Asymmetric Catalysis , pp. 1295
    • Yanagisawa, A.1    Yamamoto, H.2
  • 15
    • 16244399760 scopus 로고    scopus 로고
    • Eds, E. N. Jacobsen, A. Pfaltz, H. Yamamoto, Springer, Heidelberg
    • f) A. Yanagisawa, in: Comprehensive Asymmetric Catalysis, Suppl. 2, (Eds.: E. N. Jacobsen, A. Pfaltz, H. Yamamoto), Springer, Heidelberg, 2004, p. 125.
    • (2004) Comprehensive Asymmetric Catalysis , Issue.SUPPL. 2 , pp. 125
    • Yanagisawa, A.1
  • 16
    • 34547232810 scopus 로고    scopus 로고
    • For a recent example of catalytic asymmetric protonation of silyl enol ethers, see
    • For a recent example of catalytic asymmetric protonation of silyl enol ethers, see: A. Yanagisawa, T. Touge, T. Arai, Angew. Chem. 2005, 111, 3916;
    • (2005) Angew. Chem , vol.111 , pp. 3916
    • Yanagisawa, A.1    Touge, T.2    Arai, T.3
  • 17
    • 16244391157 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 1546.
    • (2005) Chem. Int. Ed , vol.44 , pp. 1546
    • Angew1
  • 18
    • 33748361789 scopus 로고    scopus 로고
    • For a palladium-catalyzed asymmetric decarboxylative protonation
    • For a palladium-catalyzed asymmetric decarboxylative protonation: J. T. Mohr, T. Nishimata, D.C. Behenna, B. M. Stoltz, J. Am. Chem. Soc. 2006, 125, 11348.
    • (2006) J. Am. Chem. Soc , vol.125 , pp. 11348
    • Mohr, J.T.1    Nishimata, T.2    Behenna, D.C.3    Stoltz, B.M.4
  • 19
    • 0034975355 scopus 로고    scopus 로고
    • For reviews, see: a
    • For reviews, see: a) T. Hayashi, Synlett 2001, 879;
    • (2001) Synlett , pp. 879
    • Hayashi, T.1
  • 21
  • 27
    • 34547215036 scopus 로고    scopus 로고
    • For examples of catalytic asymmetric 1,4-addition to quinone monoketals, see: by copper catalyst: a B. L. Feringa, M. Pineschi, L. A. Arnold, R. Imbos, A. H. M. de Vries, Angew. Chem. 1997, 109, 2733;
    • For examples of catalytic asymmetric 1,4-addition to quinone monoketals, see: by copper catalyst: a) B. L. Feringa, M. Pineschi, L. A. Arnold, R. Imbos, A. H. M. de Vries, Angew. Chem. 1997, 109, 2733;
  • 39
    • 21244442016 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2005, 44, 3909;
    • (2005) Chem. Int. Ed , vol.44 , pp. 3909
    • Angew1
  • 58
    • 34547166183 scopus 로고    scopus 로고
    • [11b]
    • [11b]


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.