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Volumn 65, Issue 10, 2000, Pages 2863-2869

Further studies of the thermal and photochemical Diels-Alder reactions of N-methyl-1,2,4-triazoline-3,5-dione (MeTAD) with naphthalene and some substituted naphthalenes

Author keywords

[No Author keywords available]

Indexed keywords

NAPHTHALENE DERIVATIVE; TRIAZOLINE DERIVATIVE;

EID: 0034685726     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo9906429     Document Type: Article
Times cited : (41)

References (30)
  • 13
    • 0343461074 scopus 로고    scopus 로고
    • 3
    • 3.
  • 14
    • 0000866826 scopus 로고
    • The alkene 2,3-dimethyl-2-butene reacts rapidly and quantitatively with MeTAD in an ene reaction to afford a relatively inert urazole product. See: Ohashi, S.; Leong, K.-W.; Matyjaszewski, K.; Butler, G. J. Org. Chem. 1980, 45, 3467.
    • (1980) J. Org. Chem. , vol.45 , pp. 3467
    • Ohashi, S.1    Leong, K.-W.2    Matyjaszewski, K.3    Butler, G.4
  • 18
    • 0342591080 scopus 로고    scopus 로고
    • max of the charge-transfer complexes of MeTAD with 6 and 8 relative to that of 2 (35 and 16 nm, respectively) correlate well with the corresponding shifts reported for the TCNE complexes of these same compounds (36 and 25 nm, respectively). See ref 18
    • max of the charge-transfer complexes of MeTAD with 6 and 8 relative to that of 2 (35 and 16 nm, respectively) correlate well with the corresponding shifts reported for the TCNE complexes of these same compounds (36 and 25 nm, respectively). See ref 18.
  • 19
    • 0343025312 scopus 로고    scopus 로고
    • Sheridan (ref la) provided some initial experimental results on this reaction
    • Sheridan (ref la) provided some initial experimental results on this reaction.
  • 26
    • 0001240249 scopus 로고
    • The stabilizing effect of a 2- and 5-methyl substituent toward cycloreversion has also been observed in a series of 1,4-endoperoxides formed via singlet oxygenation of 1,4-dimethylnaphthalene, 1,4,5-trimethylnaphthalene, and 1,2,4-trimethylnaphthalene. See ref 7a and also: Turro, N. J.; Chow, M.-F.; Rigaudy, J. J. Am. Chem. Soc. 1981, 103, 7218.
    • (1981) J. Am. Chem. Soc. , vol.103 , pp. 7218
    • Turro, N.J.1    Chow, M.-F.2    Rigaudy, J.3
  • 27
    • 0343025308 scopus 로고    scopus 로고
    • MM2 calculations performed with CS Chem3D Pro, Cambridge-Soft Corporation
    • MM2 calculations performed with CS Chem3D Pro, Cambridge-Soft Corporation.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.