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Volumn 73, Issue 1, 2008, Pages 184-190

Oxa-ene reaction of enols of amides with 4-phenyl-1,2,4-triazoline-3,5- dione

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOADDUCTS; ENOLS OF AMIDES; HYDROXYL PROTON LOSS; OXA ENE REACTIONS;

EID: 37549068060     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo702083u     Document Type: Article
Times cited : (10)

References (56)
  • 1
    • 37549015057 scopus 로고    scopus 로고
    • Preliminary report: Basheer, A.; Rappoport, Z. The 69th Meeting of the Israel Chemical Society, Tel Aviv, Israel, February 2-3, 2004, Abstract PB116.
    • Preliminary report: Basheer, A.; Rappoport, Z. The 69th Meeting of the Israel Chemical Society, Tel Aviv, Israel, February 2-3, 2004, Abstract PB116.
  • 18
    • 0009486259 scopus 로고    scopus 로고
    • Koerner v Gustorf, E.; White, D. V.; Kim, B.; Hess, D.; Leitich, J. J. Org. Chem. 1970, 35, 1155.
    • (b) Koerner v Gustorf, E.; White, D. V.; Kim, B.; Hess, D.; Leitich, J. J. Org. Chem. 1970, 35, 1155.
  • 24
    • 37549027404 scopus 로고    scopus 로고
    • Elimination of water from 4 will give a substituted 3-imino-1,5-diazabicyclo[3.2.0]heptane derivative.
    • Elimination of water from 4 will give a substituted 3-imino-1,5-diazabicyclo[3.2.0]heptane derivative.
  • 49
    • 37549011175 scopus 로고    scopus 로고
    • and see: de Mayo, P. Acc. Chem. Res. 1971, 4, 7.
    • and see: de Mayo, P. Acc. Chem. Res. 1971, 4, 7.
  • 53
    • 37549000342 scopus 로고    scopus 로고
    • We note that if the reaction proceeds via 2, 2- can also be formed initially from 1
    • - can also be formed initially from 1.
  • 54
    • 0000499168 scopus 로고    scopus 로고
    • For a stepwise mechanism in the ene reaction of 3, see: Elemes, Y.; Foote, C. S. J. Am. Chem. Soc. 1992, 114, 6044.
    • For a stepwise mechanism in the ene reaction of 3, see: Elemes, Y.; Foote, C. S. J. Am. Chem. Soc. 1992, 114, 6044.
  • 55
    • 0033596296 scopus 로고    scopus 로고
    • For aziridinium imides as innocent bystanders in the ene reaction, see
    • For aziridinium imides as "innocent bystanders" in the ene reaction, see: Singleton, D. A.; Hang, C. J. Am. Chem. Soc. 1999, 121, 11885.
    • (1999) J. Am. Chem. Soc , vol.121 , pp. 11885
    • Singleton, D.A.1    Hang, C.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.