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Volumn 14, Issue 7, 2003, Pages 787-790

A highly regio-, diastereo- and enantioselective intramolecular cyclopropanation reaction of a racemic α-diazo ketone catalyzed by chiral ortho-metalated dirhodium(II) compounds

Author keywords

[No Author keywords available]

Indexed keywords

1 DIAZO 6 METHYL 3 (2 PROPENYL) 5 HEPTEN 2 ONE; ALPHA DIAZO KETONE; KETONE DERIVATIVE; PHOSPHINE DERIVATIVE; RHODIUM COMPLEX; UNCLASSIFIED DRUG;

EID: 0037418798     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0957-4166(02)00870-4     Document Type: Article
Times cited : (12)

References (25)
  • 5
    • 0003445429 scopus 로고    scopus 로고
    • E.N. Jacobsen, A. Pfaltz, & H. Yamamoto. New York: Springer
    • Pfaltz A. Jacobsen E.N., Pfaltz A., Yamamoto H. Comprehensive Asymmetric Catalysis. 1999;513-538 Springer, New York.
    • (1999) Comprehensive Asymmetric Catalysis , pp. 513-538
    • Pfaltz, A.1
  • 6
    • 0003445429 scopus 로고    scopus 로고
    • E.N. Jacobsen, A. Pfaltz, & H. Yamamoto. New York: Springer
    • Aratani T. Jacobsen E.N., Pfaltz A., Yamamoto H. Comprehensive Asymmetric Catalysis. 1999;1451-1460 Springer, New York.
    • (1999) Comprehensive Asymmetric Catalysis , pp. 1451-1460
    • Aratani, T.1
  • 21
    • 85031201336 scopus 로고    scopus 로고
    • note
    • We assigned the stereochemistry of compound 4 as syn by comparison of the chemical shift of the endo proton attached to the methylene carbon of the cyclopropane ring with those reported for the corresponding protons of C-3 unsubstituted and C-3 propyl substituted analogues. Significant upfield shifts of the signals are seen for syn substitution (see Ref. 13).
  • 25
    • 85031195163 scopus 로고    scopus 로고
    • note
    • 2: C, 58.76; H, 4.23; N, 2.45. Found: C, 57.86; H, 4.60; N, 2.36%.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.