메뉴 건너뛰기




Volumn 62, Issue 46, 2006, Pages 10676-10682

Unusual endoperoxide isomerizations: a convenient entry into 2-vinyl-2-cyclopentenones from saturated fulvene endoperoxides

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOPENTENONE DERIVATIVE; ENDOPEROXIDE;

EID: 33749251504     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2006.07.107     Document Type: Article
Times cited : (21)

References (30)
  • 1
    • 0004007495 scopus 로고
    • Wasserman H.H., and Murray R.W. (Eds), Academic, New York, NY
    • In: Wasserman H.H., and Murray R.W. (Eds). Singlet Oxygen (1979), Academic, New York, NY
    • (1979) Singlet Oxygen
  • 20
    • 84948503533 scopus 로고
    • For a review on Jasmonoids, see:
    • For a review on Jasmonoids, see:. Ho T.-L. Synth. Commun. 4 (1974) 265
    • (1974) Synth. Commun. , vol.4 , pp. 265
    • Ho, T.-L.1
  • 23
    • 33749263673 scopus 로고    scopus 로고
    • note
    • Though 2(3H)-oxepinones are the sole products from thermal isomerizations of unsaturated fulvene endoperoxides in aprotic, non-nucleophilic solvents, 57 has been reported to give rise to considerable amounts of 58 in methanol; see Refs. 23 and 24.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.