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Volumn 38, Issue 2, 1997, Pages 295-298

Synthesis of bridged cyclooctane derivatives via alkoxy radical fragmentation

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOALKANE; POLYCYCLIC HYDROCARBON;

EID: 0039479313     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(96)02296-4     Document Type: Article
Times cited : (13)

References (33)
  • 1
    • 0002174828 scopus 로고
    • Ed. Atta-ur-Rahman, Elsevier Science Publishers, N.Y.
    • Review articles on synthesis of natural products containing 8-membered ring and taxane diterpenes: a) Oishi, T.; Ohtsuka, Y., in Studies in Natural Products Chemistry, Vol. 3 (Part B), Ed. Atta-ur-Rahman, Elsevier Science Publishers, N.Y., 1989, p. 73-115;
    • (1989) Studies in Natural Products Chemistry , vol.3 , Issue.PART B , pp. 73-115
    • Oishi, T.1    Ohtsuka, Y.2
  • 2
    • 0001985832 scopus 로고
    • Ed. Atta-ur-Rahman, Elsevier Science Publishers, N.Y.
    • b) Paquette, L.A. in: Studies in Natural Products Chemistry, Vol. 11 (Part G), Ed. Atta-ur-Rahman, Elsevier Science Publishers, N.Y., 1992, p. 3-69;
    • (1992) Studies in Natural Products Chemistry , vol.11 , Issue.PART G , pp. 3-69
    • Paquette, L.A.1
  • 3
    • 84989599265 scopus 로고
    • Ed. Atta-ur-Rahman, Elsevier Science Publishers, N.Y.
    • c) Swindell, C.S. in: Studies in Natural Products Chemistry, Vol. 12 (Part H), Ed. Atta-ur-Rahman, Elsevier Science Publishers, N.Y., 1993, p. 179-231;
    • (1993) Studies in Natural Products Chemistry , vol.12 , Issue.PART H , pp. 179-231
    • Swindell, C.S.1
  • 15
    • 0026629874 scopus 로고
    • g) Winkler, J.D.; Subrahmanyam, D.; Hsung, R.P. Tetrahedron 1993, 49, 291; ibid, 1992, 48, 7049-7056;
    • (1992) Tetrahedron , vol.48 , pp. 7049-7056
  • 22
    • 0342866778 scopus 로고    scopus 로고
    • ref. 1b
    • e) ref. 1b
  • 25
    • 0343301855 scopus 로고    scopus 로고
    • note
    • The stereochemistry at C-10 in 2 (camphor numbering) was deduced from NOE experiment on 3; the tertiary hydroxyl group at C-2 was tentatively assigned as exo, according to the known stereochemical course of the additions of organometallics to camphor and its derivatives.
  • 27
    • 85063243013 scopus 로고    scopus 로고
    • 13 C, HMQC, HMBC , IR, MS and microanalyses) are fully consistent with proposed structures
    • 13 C, HMQC, HMBC , IR, MS and microanalyses) are fully consistent with proposed structures.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.