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Volumn 65, Issue 4, 2009, Pages 792-797

Rearrangement of fused tetracyclic heterocycles induced by alkyl halides and formation of a new type of 'proton sponge'

Author keywords

[No Author keywords available]

Indexed keywords

1 N BENZYL 1,6 DIPHENYL 2,2,7,7 TETRAMETHYL 11,12 DIAZATETRACYCLO[4.4.0.1 3,10.1 5,8]DODECA 5(12),10 DIENE 11 IUM; 11 N (3 CHLOROALLYL) 1,6 DIPHENYL 2,2,7,7 TETRAMETHYL 11,12 DIAZATETRACYCLO[4.4.0.1 3,10.1 5,8]DODECA 5(12),10 DIENE 11 IUM; 11 N (3-CHLOROALLYL) 1,6 DI(TRIMETHYLSILYL) 2,2,7,7 TETRAMETHYL 11,12 DIAZATETRACYCLO[4.4.0.1 3,10.1 5,8]DODECA 5(12)10 DIENE 11 IUM; 11 N ALLYL 1,6 DI(TRIMETHYLSILYL) 2,2,7,7 TETRAMETHYL 11,12 DIAZATETRACYCLO[4.4.0.1 3,10.1 5,8]DODECA 5(12),10 DIENE 11 IUM BROMIDE; 11 N ALLYL 1,6 DIPHENYL 2,2,7,7 TETRAMETHYL 11,12 DIAZATETRACYCLO[4.4.0.1 3,10.1 5,8]DODECA 5(12),10 DIENE 11 IUM BROMIDE; 11 N BENZYL 1,6 DI(TRIMETHYLSILYL) 2,2,7,7 TETRAMETHYL 11,12 DIAZATETRACYCLO[4.4.0.1 3,10.1 5,8]DODECA 5(12),10 DIENE 11 IUM; 11 N BENZYL 1,6 DI(TRIMETHYLSILYL) 2,2,7,7 TETRAMETHYL 11,12 DIAZATETRACYCLO[4.4.0.1 3,10.1 5,8]DODECA 5(12),10 DIENE 11 IUM CHLORIDE; 11 N METHYL 1,6 DI(TRIMETHYLSILYL) 2,2,7,7 TETRAMETHYL 11,12 DIAZATETRACYCLO[4.4.0.1 3,10.1 5,8]DODECA 5(12),10 DIENE 11 IUM; 11 N METHYL 1,6 DIPHENYL 2,2,7,7 TETRAMETHYL 11,12 DIAZATETRACYCLO[4.4.0.1 3,10.1 5,8]DODECA 5(12),10 DIENE 11 IUM; 11,12 N,N' DIALLYL 1,6 DIPHENYL 2,2,7,7 TETRAMETHYL 11,12 DIAZATETRACYCLO [4.4.0.1 3,10.1 5,8]DODECANE 11 IUM BROMIDE; 11,12 N,N' DIBENZYL 1,6 DIPHENYL 2,2,7,7 TETRAMETHYL 11,12 DIAZATETRACYCLO [4.4.0.1 3,10.1 5,8]DODECANE 11 IUM; ALKADIENE; NITROGEN; PROTON; UNCLASSIFIED DRUG; XYLENE;

EID: 57649099995     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2008.11.057     Document Type: Article
Times cited : (21)

References (20)
  • 3
    • 0000349036 scopus 로고
    • Azomethine Imines
    • Padwa A. (Ed), Willey, New York, NY
    • Grashey R. Azomethine Imines. In: Padwa A. (Ed). 1,3-Dipolar Cycloaddition Chemistry (1984), Willey, New York, NY 757-763
    • (1984) 1,3-Dipolar Cycloaddition Chemistry , pp. 757-763
    • Grashey, R.1
  • 19
    • 57649096547 scopus 로고    scopus 로고
    • note
    • Xcalibur CCD System, CrysAlis Software System, Version 1.170. Oxford, England.
  • 20
    • 0004150157 scopus 로고    scopus 로고
    • Bruker AXS, Madison, WI, USA
    • Shelxtl, Version 5.10 (1997), Bruker AXS, Madison, WI, USA
    • (1997) Shelxtl, Version 5.10


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.