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Volumn 61, Issue 26, 2005, Pages 6368-6378

The effect of pre-existing stereocenters in the intramolecular asymmetric Stetter reaction

Author keywords

Cyclopentanones; Stereoselective; Stetter reaction

Indexed keywords

CYCLOPENTANONE DERIVATIVE;

EID: 20444450149     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2005.03.121     Document Type: Article
Times cited : (51)

References (24)
  • 3
    • 0001070365 scopus 로고
    • L.A. Paquette Wiley New York
    • The Stetter reaction: (a) H. Stetter, and H. Kuhlmann L.A. Paquette Organic Reactions Vol. 40 1991 Wiley New York 407 496
    • (1991) Organic Reactions , vol.40 , pp. 407-496
    • Stetter, H.1    Kuhlmann, H.2
  • 5
    • 0028845178 scopus 로고
    • Intramolecular Stetter: E. Ciganek Synthesis 1995 1311 1314
    • (1995) Synthesis , pp. 1311-1314
    • Ciganek, E.1
  • 11
    • 85050296727 scopus 로고
    • E.L. Eliel J.C. Fiaud Wiley New York
    • Kinetic Resolution Reviews: (a) H.B. Kagan, and J.C. Fiaud E.L. Eliel J.C. Fiaud Top. Stereochem. Vol. 18 1988 Wiley New York 249 330
    • (1988) Top. Stereochem. , vol.18 , pp. 249-330
    • Kagan, H.B.1    Fiaud, J.C.2
  • 14
    • 0031003909 scopus 로고    scopus 로고
    • Vedejs has coined and defined the term parallel kinetic resolution. Included in this definition is the following statement: 'Another PKR application is inherent in reactions where two enantiomers of a racemic substrate are selectively converted into separable, chiral products (regioisomers, diastereoisomers, etc.) by a single chiral reagent or catalyst.' See: E. Vedejs, and X. Chen J. Am. Chem. Soc. 119 1997 2584 2585
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 2584-2585
    • Vedejs, E.1    Chen, X.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.