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Volumn 53, Issue 48, 2014, Pages 13244-13247

Construction of axial chirality by rhodium-catalyzed asymmetric dehydrogenative heck coupling of biaryl compounds with alkenes

Author keywords

Asymmetric catalysis; Biaryls; C H activation; Chirality; Rhodium

Indexed keywords

ACTIVATION ANALYSIS; CATALYSIS; CHIRALITY; ENANTIOSELECTIVITY; RHODIUM;

EID: 84915748779     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201408805     Document Type: Article
Times cited : (248)

References (70)
  • 3
    • 0000718373 scopus 로고    scopus 로고
    • b) L. Pu, Chem. Rev. 1998, 98, 2405-2494;
    • (1998) Chem. Rev , vol.98 , pp. 2405-2494
    • Pu, L.1
  • 9
    • 2042507954 scopus 로고
    • For selected reviews, see: a) N. Miyaura, A. Suzuki, Chem. Rev. 1995, 95, 2457-2483;
    • (1995) Chem. Rev , vol.95 , pp. 2457-2483
    • Miyaura, N.1    Suzuki, A.2
  • 12
    • 22844434133 scopus 로고    scopus 로고
    • Angew. Chem. 2005, 117, 4516-4563;
    • (2005) Angew. Chem , vol.117 , pp. 4516-4563
  • 14
    • 0008757162 scopus 로고    scopus 로고
    • For selected asymmetric desymmetrization of prochiral biaryl compounds, see: a) T. Harada, T. M. T. Tuyet, A. Oku, Org. Lett. 2000, 2, 1319-1322;
    • (2000) Org. Lett , vol.2 , pp. 1319-1322
    • Harada, T.1    Tuyet, T.M.T.2    Oku, A.3
  • 20
    • 77956683709 scopus 로고    scopus 로고
    • For a review, see: a) H. Wang, Chirality 2010, 22, 827-837.
    • (2010) Chirality , vol.22 , pp. 827-837
    • Wang, H.1
  • 22
    • 0347659586 scopus 로고    scopus 로고
    • Angew. Chem. 2002, 114, 4714-4717;
    • (2002) Angew. Chem , vol.114 , pp. 4714-4717
  • 26
    • 67650079001 scopus 로고    scopus 로고
    • For a review on atroposelective [2+2+2] cycloaddition, see: a) K. Tanaka, Chem. Asian J. 2009, 4, 508-518;
    • (2009) Chem. Asian J , vol.4 , pp. 508-518
    • Tanaka, K.1
  • 35
    • 77957204974 scopus 로고    scopus 로고
    • For selected reviews on rhodium/(III)-catalyzed C-H functionalization, see: e) T. Satoh, M. Miura, Chem. Eur. J. 2010, 16, 11212-11222;
    • (2010) Chem. Eur. J , vol.16 , pp. 11212-11222
    • Satoh, T.1    Miura, M.2
  • 46
    • 84905457079 scopus 로고    scopus 로고
    • For a recent report on palladium-catalyzed intermolecular direct C-H bond iodination of biaryl compounds by kinetic resolution from our group, see: D.-W. Gao, Q. Gu, S.-L. You, ACS Catal. 2014, 4, 2741-2745.
    • (2014) ACS Catal , vol.4 , pp. 2741-2745
    • Gao, D.-W.1    Gu, Q.2    You, S.-L.3
  • 50
  • 53
    • 84895468071 scopus 로고    scopus 로고
    • Angew. Chem. 2014, 126, 517-521;
    • (2014) Angew. Chem , vol.126 , pp. 517-521
  • 55
    • 84915790629 scopus 로고    scopus 로고
    • Angew. Chem. 2014, 126, 8030-8033.
    • (2014) Angew. Chem , vol.126 , pp. 8030-8033
  • 57
    • 85081856017 scopus 로고    scopus 로고
    • CCDC 1022013 (rac-1be) and 1022014 1be (enantiopure) 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.
  • 58
    • 31444451709 scopus 로고    scopus 로고
    • For representative examples on self-disproportionation of enantiomers, see: a) V. A. Soloshonok, Angew. Chem. Int. Ed. 2006, 45, 766-769;
    • (2006) Angew. Chem. Int. Ed , vol.45 , pp. 766-769
    • Soloshonok, V.A.1
  • 59
    • 33746249657 scopus 로고    scopus 로고
    • Angew. Chem. 2006, 118, 780-783;
    • (2006) Angew. Chem , vol.118 , pp. 780-783
  • 61
  • 62
    • 13244286926 scopus 로고    scopus 로고
    • Angew. Chem. 2004, 116, 3444-3446;
    • (2004) Angew. Chem , vol.116 , pp. 3444-3446
  • 64
    • 48249145636 scopus 로고    scopus 로고
    • Angew. Chem. 2008, 120, 852-884;
    • (2008) Angew. Chem , vol.120 , pp. 852-884
  • 66
    • 54749086828 scopus 로고    scopus 로고
    • Angew. Chem. 2008, 120, 4558-4579;
    • (2008) Angew. Chem , vol.120 , pp. 4558-4579


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.