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Volumn 26, Issue 8, 1996, Pages 1555-1562

A facile synthesis of 7-methylenebicyclo-[3,3,1]nonan-3-one and its transformation leading to the novel tricyclic system, protoadamantane

Author keywords

[No Author keywords available]

Indexed keywords

ADAMANTANE DERIVATIVE; POLYCYCLIC HYDROCARBON;

EID: 0029981306     PISSN: 00397911     EISSN: None     Source Type: Journal    
DOI: 10.1080/00397919608003522     Document Type: Article
Times cited : (9)

References (32)
  • 4
    • 0002630230 scopus 로고
    • ed. Trost, B. M., Fleming, I. and Ley, S. V., Pergamon Press, Oxford, ch. 1. 1. 11
    • Crabtree, R. H. and Habib, A. "Comprehensive Organic Synthesis," ed. Trost, B. M., Fleming, I. and Ley, S. V., Pergamon Press, Oxford, 1991, vol 7, ch. 1. 1. 11;
    • (1991) Comprehensive Organic Synthesis , vol.7
    • Crabtree, R.H.1    Habib, A.2
  • 5
    • 0004174564 scopus 로고
    • ed. Baumstark, A. L., JAI, Greenwick, CT, eh. 1
    • e) Hill, C. L. "Advances in Oxygenated Processes" ed. Baumstark, A. L., JAI, Greenwick, CT, 1989, vol 1, eh. 1;
    • (1989) Advances in Oxygenated Processes , vol.1
    • Hill, C.L.1
  • 17
    • 1542733818 scopus 로고
    • ed. Noland, W. E., John Wiley and Sons, New York, and references cited therein
    • f) Cohen, Z., Varkony, H., Keinan, E. and Mazur, Y. "Organic Syntheses," Coll. Vol. VI, ed. Noland, W. E., John Wiley and Sons, New York, 1988, pp. 43-47, and references cited therein.
    • (1988) Organic Syntheses , vol.6 COLL. VOL , pp. 43-47
    • Cohen, Z.1    Varkony, H.2    Keinan, E.3    Mazur, Y.4
  • 18
    • 0014499295 scopus 로고
    • Gagneux, A. R. and Meier, R. Tetrahedron Lett. 1969, 1365. Enone 2 has been prepared mainly by the alkaline-induced fragmentation of 1,3-dibromoadamantane: the process, however, needs a steel bomb.
    • (1969) Tetrahedron Lett. , vol.1365
    • Gagneux, A.R.1    Meier, R.2
  • 20
    • 0008403828 scopus 로고
    • and references cited therein
    • Olah, G. A., Krishnamurti, R. and Prakash, G. K. S. Synthesis 1990, 646; Stetter, H., Gärtner, J. and Tacke, P. Chem. Ber. 1965, 98, 3888, and references cited therein.
    • (1965) Chem. Ber. , vol.98 , pp. 3888
    • Stetter, H.1    Gärtner, J.2    Tacke, P.3
  • 28
    • 0001164243 scopus 로고
    • Conversion of 7 to 8 by the direct hydroxylation has been reported, but with low conversion rate, see, Cohen, Z., Keinan, E., Mazur, Y. and Varkony, T. H. J. Org. Chem. 1975, 40, 2141.
    • (1975) J. Org. Chem. , vol.40 , pp. 2141
    • Cohen, Z.1    Keinan, E.2    Mazur, Y.3    Varkony, T.H.4
  • 30
    • 34248196388 scopus 로고
    • ed. Noland, W. E., John Wiley and Sons, New York
    • Majerski, Z. and Hamersak, Z. "Organic. Syntheses," Coll. Vol. VI, ed. Noland, W. E., John Wiley and Sons, New York, 1988, pp. 958-962.
    • (1988) Organic. Syntheses , vol.6 COLL. VOL , pp. 958-962
    • Majerski, Z.1    Hamersak, Z.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.