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Volumn 58, Issue 40, 2002, Pages 8067-8071

Study on direct benzoannelations of pyrrole and indole systems by domino reactions with 4,5-dicyanopyridazine

Author keywords

4,5 dicyanopyridazine; Cycloadditions; Domino processes; Pyrrole, indole and carbazole derivatives

Indexed keywords

4,5 DICYANOPYRIDAZINE; INDOLE; NITROGEN; PYRIDAZINE DERIVATIVE; PYRROLE; UNCLASSIFIED DRUG;

EID: 0037201493     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(02)00958-4     Document Type: Article
Times cited : (24)

References (38)
  • 1
    • 84943388739 scopus 로고
    • Pyrroles and their Benzo Derivatives: Synthesis and Applications
    • C.W. Bird, & G.W.H. Cheeseman. Pergamon, Oxford
    • (a) Sundberg R.J. Pyrroles and their Benzo Derivatives: Synthesis and Applications. Bird C.W., Cheeseman G.W.H., Comprehensive Heterocyclic Chemistry. Vol. 4:1984;313-376 Pergamon, Oxford,
    • (1984) Comprehensive Heterocyclic Chemistry , vol.4 , pp. 313-376
    • Sundberg, R.J.1
  • 2
    • 0001426611 scopus 로고    scopus 로고
    • Pyrroles and their Benzo Derivatives: Synthesis
    • Bird C.W.; Pergamon, Oxford
    • (b) Sundberg R.J. Pyrroles and their Benzo Derivatives: Synthesis. Bird C.W., Comprehensive Heterocyclic Chemistry II. Vol. 2:1996;119-206 Pergamon, Oxford,
    • (1996) Comprehensive Heterocyclic Chemistry II , vol.2 , pp. 119-206
    • Sundberg, R.J.1
  • 4
    • 0011086883 scopus 로고    scopus 로고
    • Quinodimethane derivatives are not considered
    • Quinodimethane derivatives are not considered.
  • 6
    • 0011121883 scopus 로고    scopus 로고
    • Synthetic Elaboration of Indole Derivatives using Cycloaddition Reactions
    • O. Meth-Cohn. London: Academic Chapter 16
    • (a) Sundberg R.J. Synthetic Elaboration of Indole Derivatives using Cycloaddition Reactions. Meth-Cohn O., Indoles. 1996;Academic, London. Chapter 16
    • (1996) Indoles
    • Sundberg, R.J.1
  • 29
    • 0011155920 scopus 로고    scopus 로고
    • The stereochemistry of 3 is portrayed arbitrarily
    • The stereochemistry of 3 is portrayed arbitrarily.
  • 30
    • 7044235263 scopus 로고    scopus 로고
    • For a proper definition and classification of domino reactions, see: Tietze L.F. Chem. Rev. 96:1996;115-136.
    • (1996) Chem. Rev. , vol.96 , pp. 115-136
    • Tietze, L.F.1
  • 32
    • 0011111580 scopus 로고    scopus 로고
    • A positive effect of this co-reagent was previously observed for the reaction of 1 with styrene. See Ref. 11a
    • A positive effect of this co-reagent was previously observed for the reaction of 1 with styrene. See Ref. 11a.
  • 34
    • 0011148923 scopus 로고    scopus 로고
    • * level of theory using the Spartan 3.1 program, Wavefunction, Inc
    • * level of theory using the Spartan 3.1 program, Wavefunction, Inc.
  • 35
    • 0000641028 scopus 로고
    • For coupling reactions carried out under similar conditions, see: (a) Sakamoto T., Arakida H., Edo K., Yamanaka H. Heterocycles. 16:1981;965-968 (b) Sakamoto T., Arakida H., Edo K., Yamanaka H. Chem. Pharm. Bull. 30:1982;3647-3656.
    • (1981) Heterocycles , vol.16 , pp. 965-968
    • Sakamoto, T.1    Arakida, H.2    Edo, K.3    Yamanaka, H.4
  • 36
    • 85008035251 scopus 로고
    • For coupling reactions carried out under similar conditions, see: (a) Sakamoto T., Arakida H., Edo K., Yamanaka H. Heterocycles. 16:1981;965-968 (b) Sakamoto T., Arakida H., Edo K., Yamanaka H. Chem. Pharm. Bull. 30:1982;3647-3656.
    • (1982) Chem. Pharm. Bull. , vol.30 , pp. 3647-3656
    • Sakamoto, T.1    Arakida, H.2    Edo, K.3    Yamanaka, H.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.