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Volumn 62, Issue 52, 2006, Pages 12281-12287

Nucleophilic aromatic substitutions on 4,5-dicyanopyridazine. Pyrrole and indole systems as carbon nucleophiles

Author keywords

1,4 Dihydropyridazine adducts; 4,5 Dicyanopyridazine; Addition elimination processes; Nucleophilic aromatic substitutions; Pyrrole and indole nucleophiles; Pyrrolylpyridazines and indolylpyridazines

Indexed keywords

4,5 DICYANOPYRIDAZINE; ACETIC ACID; CARBON; INDOLE; PYRIDAZINE DERIVATIVE; PYRROLE; UNCLASSIFIED DRUG;

EID: 33751087492     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2006.10.007     Document Type: Article
Times cited : (16)

References (24)
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    • Pyrroles and their Benzo Derivatives: Reactivity
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    • (1996) Comprehensive Heterocyclic Chemistry , vol.2 , pp. 81-83
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  • 4
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    • Bird C.W. (Ed), Pergamon, Oxford
    • Sundberg R.J. Pyrroles and their Benzo Derivatives: Synthesis. In: Bird C.W. (Ed). Comprehensive Heterocyclic Chemistry II Vol. 2 (1996), Pergamon, Oxford 193-195
    • (1996) Comprehensive Heterocyclic Chemistry II , vol.2 , pp. 193-195
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  • 5
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    • 1,2,4,5-Tetrazines
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    • Sauer J. 1,2,4,5-Tetrazines. In: Boulton A.J. (Ed). Comprehensive Heterocyclic Chemistry II Vol. 6 (1996), Pergamon, Oxford 913-944
    • (1996) Comprehensive Heterocyclic Chemistry II , vol.6 , pp. 913-944
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  • 6
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    • 1,2,4-Triazines and their Benzo Derivatives
    • Boulton A.J. (Ed), Pergamon, Oxford
    • Neunhoeffer H. 1,2,4-Triazines and their Benzo Derivatives. In: Boulton A.J. (Ed). Comprehensive Heterocyclic Chemistry II Vol. 6 (1996), Pergamon, Oxford 533-538
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  • 22
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    • note
    • Hartree-Fock molecular orbital calculations were performed at the 3-21G* level of theory using PC Spartan pro program, Wavefunction, Inc.
  • 23
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    • note
    • For a previous syntheses of 11 and 12 from 1 and 10, operating in the presence of Pd/C, see Ref. 6.
  • 24
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    • note
    • The same conversion was also observed in the solid state, even if more slowly.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.