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Volumn 63, Issue 26, 2007, Pages 6004-6014

Tandem inverse electron demand Diels-Alder, retro-Diels-Alder and intramolecular Diels-Alder sequences: one-pot synthesis of diaza-polycycles

Author keywords

Cascade or tandem processes; Diaza polycycles; Diels Alder reactions; IMDA; Inverse electron demand; Substituted 1,2,4 triazines

Indexed keywords

1,2,4 TRIAZINE DERIVATIVE; ALLYL COMPOUND; AMINE; CARBONYL DERIVATIVE; CYCLOBUTANONE DERIVATIVE; CYCLOHEXANONE; CYCLOPENTANONE DERIVATIVE; ENAMINE; KETONE; NITROGEN; PYRROLE DERIVATIVE; TRIAZINE DERIVATIVE;

EID: 34248674881     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2007.02.056     Document Type: Article
Times cited : (32)

References (48)
  • 1
    • 34248676453 scopus 로고    scopus 로고
    • For reviews see:
  • 2
    • 84944041959 scopus 로고    scopus 로고
    • Katritzky A.R., Rees C.W., and Scriven E.F.V. (Eds), Pergamon, Oxford
    • Neunhoeffer H. In: Katritzky A.R., Rees C.W., and Scriven E.F.V. (Eds). Comprehensive Heterocyclic Chemistry II Vol. 6 (1996), Pergamon, Oxford 507-573
    • (1996) Comprehensive Heterocyclic Chemistry II , vol.6 , pp. 507-573
    • Neunhoeffer, H.1
  • 3
    • 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
  • 4
    • 34248630670 scopus 로고    scopus 로고
    • For recent examples see:
  • 7
    • 34248645295 scopus 로고    scopus 로고
    • For recent applications of triazines see:
  • 13
    • 34248666593 scopus 로고    scopus 로고
    • For reviews covering the cycloaddition reactions of heterocyclic azadienes see:
  • 17
    • 34248632684 scopus 로고    scopus 로고
    • For pyridine synthesis see Ref. 3 and:
  • 21
    • 34248653355 scopus 로고    scopus 로고
    • For recent examples see:
  • 26
    • 0023626567 scopus 로고
    • and references therein
    • Taylor E.C., and Macor J.E. J. Org. Chem. 52 (1987) 4280-4287 and references therein
    • (1987) J. Org. Chem. , vol.52 , pp. 4280-4287
    • Taylor, E.C.1    Macor, J.E.2
  • 30
  • 41
    • 34248659024 scopus 로고    scopus 로고
    • note
    • 9 the data and yields for compounds 6i and 6j were inadvertently confused (the name and data for 6j were wrongly associated with structure 6i): this is now clarified in Section 9.
  • 46
    • 0001030980 scopus 로고    scopus 로고
    • Geranyl(methyl)amine:
    • Geranyl(methyl)amine:. Doyle M.P., and Kalinin A.V. J. Org. Chem. 61 (1996) 2179-2184
    • (1996) J. Org. Chem. , vol.61 , pp. 2179-2184
    • Doyle, M.P.1    Kalinin, A.V.2
  • 47
    • 0029928856 scopus 로고    scopus 로고
    • Benzyl(but-3-enyl)amine: Similar reductive amination procedures were employed to prepare [3-(4-methoxyphenyl)allyl]methylamine
    • Benzyl(but-3-enyl)amine:. Miller M.L., and Ray P.S. Tetrahedron 52 (1996) 5739-5744 Similar reductive amination procedures were employed to prepare [3-(4-methoxyphenyl)allyl]methylamine
    • (1996) Tetrahedron , vol.52 , pp. 5739-5744
    • Miller, M.L.1    Ray, P.S.2
  • 48
    • 34248658132 scopus 로고    scopus 로고
    • note
    • CCDC 244632 contains the supplementary crystallographic data for compound 6m. These can be obtained free of charge via www.ccdc.cam.ac.uk/data_request/cif or by emailing to www.ccdc.cam.ac.uk.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.