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Volumn 37, Issue 46, 1996, Pages 8337-8340

Intermolecular chemistry of a cyclopropylcarbene and its mechanistic implications

Author keywords

[No Author keywords available]

Indexed keywords

ALKENE DERIVATIVE; CYCLOPROPANE DERIVATIVE;

EID: 0030580309     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4039(96)01906-5     Document Type: Article
Times cited : (18)

References (40)
  • 5
    • 0000129423 scopus 로고
    • 4. Ho, G. J.; Krogh-Jespersen, K.; Moss, R. A.; Shen, S.; Sheridan, R. S. and Subramanian, R.; J. Am. Chem Soc. 1989, 111, 6875. Moss, R. A.; Ho, G.-J.; Shen, S. and Krogh-Jespersen, K.; J. Am. Chem. Soc. 1990, 112, 1638.
    • (1990) J. Am. Chem. Soc. , vol.112 , pp. 1638
    • Moss, R.A.1    Ho, G.-J.2    Shen, S.3    Krogh-Jespersen, K.4
  • 10
    • 0000205967 scopus 로고
    • and references therein
    • b)Frey, H. M.; Pure and Appl. Chem. 1964, 9, 527, and references therein. These authors recognized that rearrangement and product formation in the diazirine excited state explained their data but they did not speculate on the details of this process.
    • (1964) Pure and Appl. Chem. , vol.9 , pp. 527
    • Frey, H.M.1
  • 24
    • 0011913949 scopus 로고    scopus 로고
    • Private conversation from Prof. J. Warkentin, McMaster University
    • 15. Private conversation from Prof. J. Warkentin, McMaster University.
  • 32
    • 0000767511 scopus 로고
    • ( Houben-Weyl), Regitz, M. Ed.; G. Thieme Verlag: Stuttgart
    • 20. a)Arct, J.; Brinker, U. H.; Methoden den Organishe Chemie ( Houben-Weyl), Regitz, M. Ed.; G. Thieme Verlag: Stuttgart, 1989, Vol. E19b, pp.337-375.
    • (1989) Methoden Den Organishe Chemie , vol.E19B , pp. 337-375
    • Arct, J.1    Brinker, U.H.2
  • 34
    • 0011834798 scopus 로고    scopus 로고
    • Smith, J. A.; Dissertation Abstracts, 1965, XXV, 4
    • c)Smith, J. A.; Dissertation Abstracts, 1965, XXV, 4.
  • 38
    • 85136602493 scopus 로고    scopus 로고
    • note
    • 13C NMR d 38.856, 30.351, 29.608, 28.841, 28.539, 23.617, 20.846, 20.818, 17.710, 17.407, 9.772, 7.735.
  • 39
    • 0342441460 scopus 로고
    • 22. The general diazirine synthesis of Schmitz was employed to prepare 1 except that an excess of chloramine was utilized. a) Schmitz, E.; Chem. Ber. 1962, 95, 795.
    • (1962) Chem. Ber. , vol.95 , pp. 795
    • Schmitz, E.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.