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Volumn 15, Issue 5, 2009, Pages 1205-1216

Enantioselective iridium-catalyzed allylic arylation

Author keywords

Allylic substitution asymmetric catalysis; Chiral ligands; Cross coupling; Iridium

Indexed keywords

ALLYLATION; ENANTIOSELECTIVITY; IRIDIUM; LIGANDS; SUBSTITUTION REACTIONS;

EID: 58449122728     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.200801879     Document Type: Article
Times cited : (84)

References (97)
  • 3
    • 3042695125 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2004, 43, 2426-2428;
    • (2004) Angew. Chem. Int. Ed , vol.43 , pp. 2426-2428
  • 6
    • 33748784323 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 5995-5998;
    • (2006) Angew. Chem. Int. Ed , vol.45 , pp. 5995-5998
  • 8
    • 34250847059 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2007, 46, 2619-2622;
    • (2007) Angew. Chem. Int. Ed , vol.46 , pp. 2619-2622
  • 10
    • 58449085033 scopus 로고    scopus 로고
    • Eds, A. Pfaltz, M. Lautens
    • a) B. M. Trost in Allylic substitution reactions, Vol. 2 (Eds.: A. Pfaltz, M. Lautens), 1999, pp. 833-884;
    • (1999) Allylic substitution reactions , vol.2 , pp. 833-884
    • Trost, B.M.1
  • 11
  • 12
    • 38049017956 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2008, 47, 258-297.
    • (2008) Angew. Chem. Int. Ed , vol.47 , pp. 258-297
  • 14
    • 0028903191 scopus 로고    scopus 로고
    • M. van Klaveren, E. S. M, Persson, A. del Villar, D. M.. Grove, J.-E. Bäckvall, G. van Koten, Tetrahedron Lett. 1995, 36, 3059-3062; for reviews on Cu, see:
    • M. van Klaveren, E. S. M, Persson, A. del Villar, D. M.. Grove, J.-E. Bäckvall, G. van Koten, Tetrahedron Lett. 1995, 36, 3059-3062; for reviews on Cu, see:
  • 21
    • 0042368347 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 1999, 38, 379-381;
    • (1999) Angew. Chem. Int. Ed , vol.38 , pp. 379-381
  • 24
    • 0035901668 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2001, 40, 1456-1459;.
    • (2001) Angew. Chem. Int. Ed , vol.40 , pp. 1456-1459
  • 25
    • 0035901668 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2001, 40, 1456-1459.
    • (2001) Angew. Chem. Int. Ed , vol.40 , pp. 1456-1459
  • 28
    • 34250705242 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2007, 46, 3860-3864;
    • (2007) Angew. Chem. Int. Ed , vol.46 , pp. 3860-3864
  • 46
    • 58449113955 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2007, 45, 4554-4558.
    • (2007) Angew. Chem. Int. Ed , vol.45 , pp. 4554-4558
  • 55
    • 0037176296 scopus 로고    scopus 로고
    • T. Ohmura, J. F. Hartwig, J. Am. Chem. Soc. 2002, 124, 151.64-15165.
    • T. Ohmura, J. F. Hartwig, J. Am. Chem. Soc. 2002, 124, 151.64-15165.
  • 56
    • 33846935049 scopus 로고    scopus 로고
    • For seminal reviews, see: a
    • For seminal reviews, see: a) R. Takeuchi, S. Kezuka, Synthesis 2006, 3349-3366;
    • (2006) Synthesis , pp. 3349-3366
    • Takeuchi, R.1    Kezuka, S.2
  • 61
    • 33749006910 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2006, 45, 6204-6207.
    • (2006) Angew. Chem. Int. Ed , vol.45 , pp. 6204-6207
  • 64
    • 0000749009 scopus 로고    scopus 로고
    • For the use of carbamates in allylic substitution and their beneficial effect towards regioselectivity, see: H. L. Goering, S. S. Kantner, C. C. Tseng, J. Org. Chem. 1983, 48, 715-721
    • For the use of carbamates in allylic substitution and their beneficial effect towards regioselectivity, see: H. L. Goering, S. S. Kantner, C. C. Tseng, J. Org. Chem. 1983, 48, 715-721.
  • 65
    • 58449083643 scopus 로고    scopus 로고
    • University of Geneva Switzerland
    • X. Rathgeb, PhD Dissertation, University of Geneva (Switzerland), 2007.
    • (2007)
    • Rathgeb, X.1    Dissertation, P.D.2
  • 68
    • 35048898027 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2007, 46, 7462-7465.
    • (2007) Angew. Chem. Int. Ed , vol.46 , pp. 7462-7465
  • 73
    • 0034672069 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2000, 39, 4414-4435.
    • (2000) Angew. Chem. Int. Ed , vol.39 , pp. 4414-4435
  • 76
    • 0028059105 scopus 로고
    • For other enantioselective syntheses of sertraline, see: a
    • For other enantioselective syntheses of sertraline, see: a) E. J. Corey, T. J. Gant, Tetrahedron Lett. 1994, 35, 5373-5376;
    • (1994) Tetrahedron Lett , vol.35 , pp. 5373-5376
    • Corey, E.J.1    Gant, T.J.2
  • 79
    • 1942533561 scopus 로고    scopus 로고
    • to prevent the occurrence of racemization, we avoided using a palladium-catalyzed hydrogenation reaction, for details
    • M. P. Rainka, Y. Aye, S. L. Buchwald, Proc. Natl. Acad. Sci USA 2004, 101, 5821-5823; to prevent the occurrence of racemization, we avoided using a palladium-catalyzed hydrogenation reaction, for details,
    • (2004) Proc. Natl. Acad. Sci USA , vol.101 , pp. 5821-5823
    • Rainka, M.P.1    Aye, Y.2    Buchwald, S.L.3
  • 91
    • 34250847059 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2007, 46, 2619-2622.
    • (2007) Angew. Chem. Int. Ed , vol.46 , pp. 2619-2622
  • 96
    • 58449106915 scopus 로고    scopus 로고
    • K. Tissot-Croset, PhD Dissertation, University of Geneva (Switzerland), 2005.
    • K. Tissot-Croset, PhD Dissertation, University of Geneva (Switzerland), 2005.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.