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Volumn 9, Issue 11, 2007, Pages 2107-2110

Organocatalytic diastereo- And enantioselective Michael addition reactions of 5-aryl-1,3-dioxolan-4-ones

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EID: 34250626847     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol070532l     Document Type: Article
Times cited : (79)

References (41)
  • 12
    • 15444366940 scopus 로고    scopus 로고
    • For recent applications of epi-9-amino-9-deoxy cinchona alkaloid derivatives as bifunctional organocatalysts, see: a
    • For recent applications of epi-9-amino-9-deoxy cinchona alkaloid derivatives as bifunctional organocatalysts, see: (a) Li, B.; Jiang, L.; Liu, M.; Chen, Y.; Ding, L.; Wu, Y. Synlett 2005, 603.
    • (2005) Synlett , pp. 603
    • Li, B.1    Jiang, L.2    Liu, M.3    Chen, Y.4    Ding, L.5    Wu, Y.6
  • 32
    • 34247167637 scopus 로고    scopus 로고
    • 3830. For mechanistic studies utilizing the cinchona alkaloids, see
    • (u) Biddle, M. M.; Lin, M.; Scheidt, K. A. J. Am. Chem. Soc. 2007, 129, 3830. For mechanistic studies utilizing the cinchona alkaloids, see:
    • (2007) J. Am. Chem. Soc , vol.129
    • Biddle, M.M.1    Lin, M.2    Scheidt, K.A.3
  • 36
    • 0037131745 scopus 로고    scopus 로고
    • For examples of the use of chiral dioxolan-4-ones in stereoselective Michael reactions, see: (a) Blay, G, Fernández, I, Monje, B, Pedro, J. R, Ruiz, R. Tetrahedron Lett. 2002, 43, 8463
    • For examples of the use of chiral dioxolan-4-ones in stereoselective Michael reactions, see: (a) Blay, G.; Fernández, I.; Monje, B.; Pedro, J. R.; Ruiz, R. Tetrahedron Lett. 2002, 43, 8463.
  • 41
    • 34250618961 scopus 로고    scopus 로고
    • Diastereoisomers 11 and 12 were separated by preparative HPLC with use of an OJ column (see the Supporting Information for details).
    • Diastereoisomers 11 and 12 were separated by preparative HPLC with use of an OJ column (see the Supporting Information for details).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.