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Volumn 127, Issue 18, 2005, Pages 6877-6882

A readily available chiral Ag-based N-heterocyclic carbene complex for use in efficient and highly enantioselective Ru-catalyzed olefin metathesis and Cu-catalyzed allylic alkylation reactions

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOLS; ALKYLATION; CATALYSIS; COMPLEXATION; COORDINATION REACTIONS; COPPER; FREE RADICALS; ISOMERS; OLEFINS; RUTHENIUM; SILVER; STEREOCHEMISTRY; SYNTHESIS (CHEMICAL);

EID: 18644377613     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja050179j     Document Type: Article
Times cited : (346)

References (89)
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    • note
    • (a) Reference 2c.
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    • For representative reports regarding Cu-catalyzed allylic alkylations involving alkylmetal reagents, see: (a) Dubner, F.; Knochel, P. Angew. Chem., Int. Ed. 1999, 38, 379-381.
    • (1999) Angew. Chem., Int. Ed. , vol.38 , pp. 379-381
    • Dubner, F.1    Knochel, P.2
  • 51
    • 3242812738 scopus 로고    scopus 로고
    • For representative recent examples involving use of NHCs as chiral catalysts, see: (a) Kerr, M. S.; Rovis, T. J. Am. Chem. Soc. 2004, 126, 8876-8877.
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 8876-8877
    • Kerr, M.S.1    Rovis, T.2
  • 58
    • 0039772398 scopus 로고    scopus 로고
    • A chiral ligand may induce asymmetry in the coordination of a second (and achiral in the absence of metal coordination) ligand, see: (a) Ringwald, M.; Sturmer, R.; Brintzinger, H. H. J. Am. Chem. Soc. 1999, 121, 1524-1527.
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 1524-1527
    • Ringwald, M.1    Sturmer, R.2    Brintzinger, H.H.3
  • 68
    • 0000937023 scopus 로고    scopus 로고
    • Diamine 3 can be prepared in the optically pure form (both antipodes) in multigram quantities in ∼20% overall yield (five steps from benzaldehydes). Procedures leading to the preparation of optically pure diamine 3 were obtained from: (a) Kupfer, R.; Brinker, U. H. J. Org. Chem. 1996, 61, 4185-4186.
    • (1996) J. Org. Chem. , vol.61 , pp. 4185-4186
    • Kupfer, R.1    Brinker, U.H.2
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  • 81
    • 0000004671 scopus 로고    scopus 로고
    • Ag-based complexes of heterocyclic carbenes readily undergo exchange with a variety of late transition metals. See: (a) Wang, H. M. J.; Lin, I. J. B. Organometallics 1998, 77, 972-975.
    • (1998) Organometallics , vol.77 , pp. 972-975
    • Wang, H.M.J.1    Lin, I.J.B.2
  • 82
    • 0036390738 scopus 로고    scopus 로고
    • and references therein
    • (b) Arnold, P. L. Heteroat. Chem. 2002, 13, 534-539 and references therein.
    • (2002) Heteroat. Chem. , vol.13 , pp. 534-539
    • Arnold, P.L.1
  • 83
    • 0032473509 scopus 로고    scopus 로고
    • For reviews on enantioselective synthesis of quaternary carbon stereogenic centers, see: (a) Corey, E. J.; Guzman-Perez, A. Angew. Chem., Int. Ed. 1998, 37, 388-401.
    • (1998) Angew. Chem., Int. Ed. , vol.37 , pp. 388-401
    • Corey, E.J.1    Guzman-Perez, A.2
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  • 89
    • 0003134584 scopus 로고    scopus 로고
    • Jacobsen, E. N., Pfaltz, A., Yamamoto, H., Eds.; Springer: Berlin, Germany
    • For a review, see: Hoveyda, A. H.; Heron, N. M. In Comprehensive Asymmetric Catalysis; Jacobsen, E. N., Pfaltz, A., Yamamoto, H., Eds.; Springer: Berlin, Germany, 1999; pp 431-454.
    • (1999) Comprehensive Asymmetric Catalysis , pp. 431-454
    • Hoveyda, A.H.1    Heron, N.M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.