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Volumn 119, Issue 48, 1997, Pages 11605-11610

[3 + 2] Cycloadditions and protonation by alcohols of photochemically generated nitrile ylides from 2H-Azirines. Formation and reactivities of azaallenium cations

Author keywords

[No Author keywords available]

Indexed keywords

IMINE;

EID: 0031435976     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja971648n     Document Type: Article
Times cited : (40)

References (27)
  • 3
    • 0001535071 scopus 로고
    • (a) Heimgartner, H. Angew. Chem. 1991, 103, 271-297; Angew. Chem., Int. Ed. Engl. 1991, 30, 238.
    • (1991) Angew. Chem. , vol.103 , pp. 271-297
    • Heimgartner, H.1
  • 4
    • 0026021427 scopus 로고
    • (a) Heimgartner, H. Angew. Chem. 1991, 103, 271-297; Angew. Chem., Int. Ed. Engl. 1991, 30, 238.
    • (1991) Angew. Chem., Int. Ed. Engl. , vol.30 , pp. 238
  • 6
    • 0004167906 scopus 로고
    • Horspool, W. M., Ed.: Plenum Press, New York
    • (c) Padwa, A. Synthetic Organic Photochemistry; Horspool, W. M., Ed.: Plenum Press, New York, 1984; pp 313-373.
    • (1984) Synthetic Organic Photochemistry , pp. 313-373
    • Padwa, A.1
  • 16
    • 0001134069 scopus 로고
    • Nitrile ylides
    • Padwa, A., Ed.; John Wiley & Sons: New York, Ka
    • (c) Hansen, H.; Heimgartner, H. Nitrile Ylides. In 1,3-Dipolar Cycloaddition Chemistry; Padwa, A., Ed.; John Wiley & Sons: New York, 1984; Bd. 1, Kap. 2, p 208.
    • (1984) 1,3-Dipolar Cycloaddition Chemistry , vol.1 , pp. 2
    • Hansen, H.1    Heimgartner, H.2
  • 19
    • 84943701775 scopus 로고
    • For a review on orbital energy control of cycloaddition reactivity see: Sustmann, R. Pure Appl. Chem. 1974, 40, 569-593.
    • (1974) Pure Appl. Chem. , vol.40 , pp. 569-593
    • Sustmann, R.1
  • 20
    • 84889196632 scopus 로고    scopus 로고
    • note
    • + would neutralize the basic solution resulting in a decrease of conductivity.
  • 21
    • 84889182616 scopus 로고    scopus 로고
    • note
    • obs(d-CA).
  • 22
    • 84889185238 scopus 로고    scopus 로고
    • note
    • A dependence of the decay rate of the nitrile ylide from 3-(biphenyI4-yl)-2H-azirine on the acidity of the reaction medium has previously been found by Ishida et al. (ref 8d).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.