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Volumn 47, Issue 23, 2006, Pages 3865-3870

Tandem oxidation processes for the regioselective preparation of 5-substituted and 6-substituted 1,2,4-triazines

Author keywords

[No Author keywords available]

Indexed keywords

1,2,4 TRIAZINE DERIVATIVE; 2 PYRIDYLAMIDRAZONE; 2,2' BIPYRIDINE; ALPHA OXOALDEHYDE; KETOL; MANGANESE DIOXIDE; PYRIDINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 33646142992     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2006.03.178     Document Type: Article
Times cited : (22)

References (31)
  • 1
    • 84944041959 scopus 로고    scopus 로고
    • For reviews see:. Katritzky A.R., Rees C.W., and Scriven E.F.V. (Eds), Pergamon Press, Oxford
    • For reviews see:. Neunhoeffer H. In: Katritzky A.R., Rees C.W., and Scriven E.F.V. (Eds). Comprehensive Heterocyclic Chemistry II Vol. 6 (1996), Pergamon Press, Oxford 507-573
    • (1996) Comprehensive Heterocyclic Chemistry II , vol.6 , pp. 507-573
    • Neunhoeffer, H.1
  • 2
    • 33646136917 scopus 로고    scopus 로고
    • Weinreb S.M. (Ed), Thieme, Stuttgart
    • Lindsley C.W., and Layton M.E. In: Weinreb S.M. (Ed). Science of Synthesis Vol. 17 (2003), Thieme, Stuttgart 357-447
    • (2003) Science of Synthesis , vol.17 , pp. 357-447
    • Lindsley, C.W.1    Layton, M.E.2
  • 5
    • 33646155750 scopus 로고    scopus 로고
    • see also Refs. 2-5.
  • 11
    • 0003719612 scopus 로고
    • For reviews covering the cycloaddition reactions of heterocyclic azadienes see:, Academic Press, London Chapter 10, pp 300-358
    • For reviews covering the cycloaddition reactions of heterocyclic azadienes see:. Boger D.L., and Weinreb S.N. Hetero Diels-Alder Methodology in Organic Synthesis (1987), Academic Press, London Chapter 10, pp 300-358
    • (1987) Hetero Diels-Alder Methodology in Organic Synthesis
    • Boger, D.L.1    Weinreb, S.N.2
  • 14
    • 0022398192 scopus 로고
    • and references cited therein
    • Boger D.L., and Panek J.S. J. Am. Chem. Soc. 107 (1985) 5745-5754 and references cited therein
    • (1985) J. Am. Chem. Soc. , vol.107 , pp. 5745-5754
    • Boger, D.L.1    Panek, J.S.2
  • 26
    • 0026785118 scopus 로고
    • Non-commercial α-hydroxyketones were prepared from the corresponding methyl ketones using a published procedure:
    • Non-commercial α-hydroxyketones were prepared from the corresponding methyl ketones using a published procedure:. Moriarty R.M., Berglund B.A., and Penmasta R. Tetrahedron Lett. 33 (1992) 6065-6068
    • (1992) Tetrahedron Lett. , vol.33 , pp. 6065-6068
    • Moriarty, R.M.1    Berglund, B.A.2    Penmasta, R.3
  • 27
    • 33646123566 scopus 로고    scopus 로고
    • note
    • 1H NMR data.
  • 29
    • 33646163944 scopus 로고    scopus 로고
    • note
    • +, 241.1446 (3.5 ppm error)].
  • 30
    • 33646162217 scopus 로고    scopus 로고
    • note
    • Microwaves could also be employed for the second step (PhMe, 120 °C, 1 h), although the initial condensation proceeded more efficiently under thermal conditions.
  • 31
    • 33646151190 scopus 로고    scopus 로고
    • note
    • +, 273.1393 (-0.6 ppm error)].


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.