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Volumn 60, Issue 21, 1995, Pages 6872-6882

One-Pot Base-Promoted Tandem Michael Addition-Intramolecular Aldolization. Stereoselective Synthesis and Reactivity of 2-Hydroxybicyclo[3.2.1]octan-8-ones

Author keywords

[No Author keywords available]

Indexed keywords

BICYCLO[3.2.1]OCTANE DERIVATIVE;

EID: 0028810949     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo00126a044     Document Type: Article
Times cited : (77)

References (136)
  • 66
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    • For examples using the intramolecular double Michael addition see
    • For examples using the intramolecular double Michael addition see, Ihara, M.; Fukumoto, K. Angew. Chem., Int. Ed. Engl. 1993, 32, 1010.
    • (1993) Angew. Chem., Int. Ed. Engl. , vol.32 , pp. 1010
    • Ihara, M.1    Fukumoto, K.2
  • 117
    • 0024518339 scopus 로고
    • For recent successful base promoted condensative cyclizations leading to the parent bicyclo[3.3.1]nonane skeleton, see
    • For recent successful base promoted condensative cyclizations leading to the parent bicyclo[3.3.1]nonane skeleton, see: Qian, L.; Ji, R. Tetrahedron Lett. 1989, 30, 2089.
    • (1989) Tetrahedron Lett. , vol.30 , pp. 2089
    • Qian, L.1    Ji, R.2
  • 123
    • 0001460679 scopus 로고
    • For the preparation of lc from (R)-(+)-pulegone, see
    • For the preparation of lc from (R)-(+)-pulegone, see: Marx, J. N.; Norman, L. R. J. Org. Chem. 1975, 40, 1602.
    • (1975) J. Org. Chem. , vol.40 , pp. 1602
    • Marx, J.N.1    Norman, L.R.2
  • 124
    • 0014819845 scopus 로고
    • Compounds ld,e were prepared by esterification of pulegenic acid following the literature procedure
    • Compounds ld,e were prepared by esterification of pulegenic acid following the literature procedure: Murphy, C. F.; Koehler, R. E. J. Org. Chem. 1970, 35, 2429.
    • (1970) J. Org. Chem. , vol.35 , pp. 2429
    • Murphy, C.F.1    Koehler, R.E.2
  • 129
    • 0000274179 scopus 로고
    • For a model for the diastereofacial differentiation in the alkylation of related endocyclic enolates with an asymmetric center at the β-position, see
    • For a model for the diastereofacial differentiation in the alkylation of related endocyclic enolates with an asymmetric center at the β-position, see: Tomioka, K.; Kawasaki, H.; Yasuda, K.; Koga, K. J. Am. Chem. Soc. 1988, 110, 3597.
    • (1988) J. Am. Chem. Soc. , vol.110 , pp. 3597
    • Tomioka, K.1    Kawasaki, H.2    Yasuda, K.3    Koga, K.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.