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Volumn 40, Issue 8, 1999, Pages 1551-1554

Construction of bicyclo[2.2.2]octane ring system via homoallyl-homoallyl radical rearrangement

Author keywords

[No Author keywords available]

Indexed keywords

BICYCLO[2.2.2]OCTANE DERIVATIVE; CYCLOHEXENE DERIVATIVE; FREE RADICAL;

EID: 0033582602     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(98)02708-7     Document Type: Article
Times cited : (38)

References (25)
  • 8
    • 0004052210 scopus 로고
    • Eds.: S. G. Davies, Oxford University Press, New York
    • L. M. Harwood in Polar Rearrangements, Vol. 5 (Eds.: S. G. Davies), Oxford University Press, New York, 1992.
    • (1992) Polar Rearrangements , vol.5
    • Harwood, L.M.1
  • 22
    • 0013577752 scopus 로고    scopus 로고
    • note
    • 1H-COSY NMR experiments. Enhancements, shown in Figure II, were proofs of the proposed structure. This result indicates that the ratio of the products (13 and 14) depends on the stability of the intermediates (7 and 9) in the equilibration. Figure II (equation presented).
  • 25
    • 0013609085 scopus 로고    scopus 로고
    • At this stage, the other products such as monocyclized unsaturated compound were oxidized to give the corresponding carbonyl compounds. Although 35% yield, the isolation of the monobenzyl-substituted cyclopropane product is a rare case
    • At this stage, the other products such as monocyclized unsaturated compound were oxidized to give the corresponding carbonyl compounds. Although 35% yield, the isolation of the monobenzyl-substituted cyclopropane product is a rare case.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.