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Volumn 46, Issue 11, 2005, Pages 1889-1891

Synthesis, characterization, and structure of a new N-nitrosamine of cyclam (1,4,8,11-tetraazacyclotetradecane)

Author keywords

Cyclam; N Nitrosamine; NO release; Photoreactivity

Indexed keywords

CYCLAM DERIVATIVE;

EID: 13944256265     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2005.01.097     Document Type: Article
Times cited : (7)

References (19)
  • 8
    • 85030810530 scopus 로고    scopus 로고
    • note
    • 4) was bubbled through this solution during 4 h, when it was observed the precipitation of a yellow crystalline solid. The crystals were collected by filtration, washed with cold water, and dried under vacuum. Elemental analysis: Cald C: 37.97; H: 6.37; N: 35.42. Found. C: 37.69; H: 6.34; N: 35.26
  • 9
    • 85030813023 scopus 로고    scopus 로고
    • deposit@ccdc.cam.ac.uk
    • 4 have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication number CCDC 249972. Copies of the data may be obtained, free of charge, on application to CCDC, 12 Union Road, Cambridge, CB2 1EZ, U.K. (fax: +44(0)-1223-336033 or e-mail: deposit@ccdc.cam.ac.uk)
  • 10
    • 33646767009 scopus 로고    scopus 로고
    • ORTEP-3 for Windows
    • L.J. Farrugia ORTEP-3 for Windows J. Appl. Cryst. 30 1997 565 571
    • (1997) J. Appl. Cryst. , vol.30 , pp. 565-571
    • Farrugia, L.J.1
  • 19
    • 85030809410 scopus 로고    scopus 로고
    • note
    • LCMS analyses were conducted using isocratic elution (acetonitrile/water, 90:20 v/v) with a Shimadzu C18 column (250 × 2.0 mm, 4.6 μm). The experiments were carried out on a Shimadzu LCMS-2010 equipment. The measurements were performed in positive mode by scanning between m/z 50 and 400 using an APCI interface and SIM technique


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