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Volumn 45, Issue 45, 2006, Pages 7591-7595

Highly active chiral ruthenium catalysts for asymmetric cross- and ring-opening cross-metathesis

Author keywords

Asymmetric catalysis; Carbenes; Metathesis; Reaction mechanisms; Ruthenium

Indexed keywords

AROMATIC COMPOUNDS; CATALYST ACTIVITY; CATALYST SELECTIVITY; REACTION KINETICS; RUTHENIUM;

EID: 33845207666     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200602469     Document Type: Article
Times cited : (126)

References (33)
  • 1
    • 1442360753 scopus 로고    scopus 로고
    • Wiley-VCH, Weinheim
    • For recent reviews on olefin metathesis, see: a) R. H. Grubbs, Handbook of Metathesis, Wiley-VCH, Weinheim, 2003;
    • (2003) Handbook of Metathesis
    • Grubbs, R.H.1
  • 3
    • 0001399412 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2000, 39, 3012-3043;
    • (2000) Angew. Chem. Int. Ed. , vol.39 , pp. 3012-3043
  • 6
    • 1842796379 scopus 로고    scopus 로고
    • For reviews of molybdenum-catalyzed enantioselective metathesis, see: a) R. R. Schrock, A. H. Hoveyda, Angew. Chem. 2003, 115, 4740-4782;
    • (2003) Angew. Chem. , vol.115 , pp. 4740-4782
    • Schrock, R.R.1    Hoveyda, A.H.2
  • 7
    • 0142023994 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2003, 42, 4592-4633; ;
    • (2003) Angew. Chem. Int. Ed. , vol.42 , pp. 4592-4633
  • 14
    • 0035901680 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed. 2001, 40, 1452-1456.
    • (2001) Angew. Chem. Int. Ed. , vol.40 , pp. 1452-1456
  • 15
    • 33845224205 scopus 로고    scopus 로고
    • note
    • Catalysts 4a,b have not been previously reported, but were prepared analogously to 2a,b, 3a,b, 5a,b, and 6a,b. For full experimental details, see the Supporting Information.
  • 18
    • 33845197364 scopus 로고    scopus 로고
    • note
    • On comparison with the results from references [6a] and [8c].
  • 31
    • 33845206979 scopus 로고    scopus 로고
    • note
    • The absolute stereochemistry of 9 has been determined by analysis of the X-ray crystal structure of an imide derivative (see the Supporting Information). From the comparison of HPLC traces run under identical conditions,our studies indicate that the incorrect absolute stereoisomer was reported in reference [8d].


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.