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Volumn 36, Issue 3, 1999, Pages 813-818

Ring transformations of heterocyclic compounds. XVII [1]. 2-(2,4,6- triarylphenyl) substituted dihydro-1H-imidazolium, dihydrothiazolium and thiazolium salts from 2-methyl derivatives by pyrylium and thiopyrylium ring transformations

Author keywords

[No Author keywords available]

Indexed keywords

HETEROCYCLIC COMPOUND; IMIDAZOLE DERIVATIVE; THIAZOLE DERIVATIVE;

EID: 0032780110     PISSN: 0022152X     EISSN: None     Source Type: Journal    
DOI: 10.1002/jhet.5570360339     Document Type: Article
Times cited : (2)

References (36)
  • 8
    • 0001467743 scopus 로고
    • R. P. Kreher, ed, Thieme, Stuttgart
    • [b] W. Schroth, W. Dölling, and A. T. Balaban, in Houben-Weyl, Vol E7b, R. P. Kreher, ed, Thieme, Stuttgart, 1992, pp 755-1014.
    • (1992) Houben-Weyl , vol.E7B , pp. 755-1014
    • Schroth, W.1    Dölling, W.2    Balaban, A.T.3
  • 9
    • 0004664787 scopus 로고
    • R. P. Kreher, ed, Thieme, Stuttgart
    • W. Dölling and W. Schroth, in Houben-Weyl, Vol E7b, R. P. Kreher, ed, Thieme, Stuttgart, 1992, pp 687-754; G. Doddi and G. Ercolani, Adv. Heterocyclic Chem., 60, 66 (1994).
    • (1992) Houben-Weyl , vol.E7B , pp. 687-754
    • Dölling, W.1    Schroth, W.2
  • 10
    • 0003547912 scopus 로고
    • W. Dölling and W. Schroth, in Houben-Weyl, Vol E7b, R. P. Kreher, ed, Thieme, Stuttgart, 1992, pp 687-754; G. Doddi and G. Ercolani, Adv. Heterocyclic Chem., 60, 66 (1994).
    • (1994) Adv. Heterocyclic Chem. , vol.60 , pp. 66
    • Doddi, G.1    Ercolani, G.2
  • 12
    • 0040173584 scopus 로고    scopus 로고
    • O. Brede, L. Goebel, and T. Zimmermann, J. Inf. Rec. Mater., 22, 397 (1996); L. Goebel, O. Brede, and T. Zimmermann, Radiat. Phys. Chem., 47, 369 (1996); O. Brede, L. Goebel, and T. Zimmermann, J. Phys. Chem. A, 101, 4103 (1997).
    • (1996) J. Inf. Rec. Mater. , vol.22 , pp. 397
    • Brede, O.1    Goebel, L.2    Zimmermann, T.3
  • 13
    • 0030069932 scopus 로고    scopus 로고
    • O. Brede, L. Goebel, and T. Zimmermann, J. Inf. Rec. Mater., 22, 397 (1996); L. Goebel, O. Brede, and T. Zimmermann, Radiat. Phys. Chem., 47, 369 (1996); O. Brede, L. Goebel, and T. Zimmermann, J. Phys. Chem. A, 101, 4103 (1997).
    • (1996) Radiat. Phys. Chem. , vol.47 , pp. 369
    • Goebel, L.1    Brede, O.2    Zimmermann, T.3
  • 14
    • 0000745687 scopus 로고    scopus 로고
    • O. Brede, L. Goebel, and T. Zimmermann, J. Inf. Rec. Mater., 22, 397 (1996); L. Goebel, O. Brede, and T. Zimmermann, Radiat. Phys. Chem., 47, 369 (1996); O. Brede, L. Goebel, and T. Zimmermann, J. Phys. Chem. A, 101, 4103 (1997).
    • (1997) J. Phys. Chem. A , vol.101 , pp. 4103
    • Brede, O.1    Goebel, L.2    Zimmermann, T.3
  • 15
    • 0343417880 scopus 로고
    • E. Schaumann, ed, Thieme, Stuttgart
    • For a review on 1H-imidazoles and their derivatives see: K. Ebel, in Houben-Weyl, Vol E8c, E. Schaumann, ed, Thieme, Stuttgart, 1994, pp 1-215.
    • (1994) Houben-Weyl , vol.E8C , pp. 1-215
    • Ebel, K.1
  • 16
    • 0001890934 scopus 로고
    • E. Schaumann, ed, Thieme, Stuttgart
    • Review on thiazoles and their chemistry: J. Liebscher, in Houben-Weyl, Vol E8b, E. Schaumann, ed, Thieme, Stuttgart, 1994, pp 1-398.
    • (1994) Houben-Weyl , vol.E8B , pp. 1-398
    • Liebscher, J.1
  • 20
    • 0344257953 scopus 로고
    • H. Kropf and E. Schaumann, eds, Thieme, Stuttgart
    • The anhydrobases of 2 and 4 are ketene-N,N-acetals and ketene-S,N-acetals, respectively, the chemistry of which is well documented: W. Kantlehner, in Houben-Weyl, Vol E15, H. Kropf and E. Schaumann, eds, Thieme, Stuttgart, 1993, pp 1942-2347; E. Schaumann, in Houben-Weyl, Vol E11, D. Klamann, ed, Thieme, Stuttgart, 1985, pp 325-341 and references cited therein.
    • (1993) Houben-Weyl , vol.E15 , pp. 1942-2347
    • Kantlehner, W.1
  • 21
    • 0344689641 scopus 로고
    • D. Klamann, ed, Thieme, Stuttgart, and references cited therein
    • The anhydrobases of 2 and 4 are ketene-N,N-acetals and ketene-S,N-acetals, respectively, the chemistry of which is well documented: W. Kantlehner, in Houben-Weyl, Vol E15, H. Kropf and E. Schaumann, eds, Thieme, Stuttgart, 1993, pp 1942-2347; E. Schaumann, in Houben-Weyl, Vol E11, D. Klamann, ed, Thieme, Stuttgart, 1985, pp 325-341 and references cited therein.
    • (1985) Houben-Weyl , vol.E11 , pp. 325-341
    • Schaumann, E.1
  • 22
    • 0344257952 scopus 로고    scopus 로고
    • note
    • For the classification of pyrylium ring transformations see ref [7a] p 85; the same classification principle can also be applied to thiopyrylium transformations.
  • 34
    • 0344689636 scopus 로고
    • M. Yu. Kornilov, E. D. Aych, and L. I. Smeshko, Ukr. Khim. Zh., 39, 52 (1973), Chem. Abstr. 79, 17689 (1973).
    • (1973) Chem. Abstr. , vol.79 , pp. 17689


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.