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Volumn 51, Issue 1, 2015, Pages 221-224

Isoquinolino[4,3,2-de]phenanthridine: Synthesis and its use in 1,3-dipolar cycloadditions to form nitrogen-containing polyaromatic hydrocarbons

Author keywords

[No Author keywords available]

Indexed keywords

ALKENE; ALKYNE; AZOMETHINE YLIDE; FUSED PYRROLIDINE; ISOQUINOLINO[4,3,2 DE]PHENANTHRIDINE; NITROGEN; NITROGEN CONTAINING POLYAROMATIC HYDROCARBON; POLYCYCLIC AROMATIC HYDROCARBON; PYRROLE DERIVATIVE; PYRROLIDINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 84915819837     PISSN: 13597345     EISSN: 1364548X     Source Type: Journal    
DOI: 10.1039/c4cc06643j     Document Type: Article
Times cited : (59)

References (50)
  • 28
    • 72849122523 scopus 로고    scopus 로고
    • During the preparation of the present manuscript, Feng and Müllen et al. reported the synthesis of isoquinolino[4,3,2-de]phenanthridine (1) as a model segment for nitrogen-doped zigzag-edge peripheries and its use in 1,3-dipolar cycloadditions to generate 2,5-dihydropyrroles
    • D. Wu W. Pisula M. C. Haberecht X. Feng K. Müllen Org. Lett. 2009 11 5686
    • (2009) Org. Lett. , vol.11 , pp. 5686
    • Wu, D.1    Pisula, W.2    Haberecht, M.C.3    Feng, X.4    Müllen, K.5
  • 40
    • 0000034021 scopus 로고
    • Since azomethine ylides are generally unstable, only few examples of isolated azomethine ylides - typically having electron-withdrawing groups for stabilization - have so far been reported
    • C. Radlowski W. V. Sherman J. Phys. Chem. 1970 74 3043
    • (1970) J. Phys. Chem. , vol.74 , pp. 3043
    • Radlowski, C.1    Sherman, W.V.2
  • 44
    • 84980247455 scopus 로고
    • A reaction with a terminal alkyne, phenylacetylene, under the same conditions afforded a complex mixture of products
    • H. Seidl R. Huisgen R. Knorr Chem. Ber. 1969 102 904
    • (1969) Chem. Ber. , vol.102 , pp. 904
    • Seidl, H.1    Huisgen, R.2    Knorr, R.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.