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J Org Chem ; 73(18): 7159-63, 2008 Sep 19.
Article in English | MEDLINE | ID: mdl-18722411

ABSTRACT

To evaluate the ability of dibenzothiophene N-substituted sulfilimines as photochemical nitrene sources, their photolyses in the presence of several trapping reagents, such as sulfides, olefins, and phosphorus compounds, were performed. In the reactions, the corresponding imino-transfer compounds, namely sulfilimines, aziridines, and iminophosphoranes, were formed in good yields, indicating dibenzothiophene N-tosyl and N-acylsulfilimines have a potent nature as nitrogen sources.


Subject(s)
Imines/radiation effects , Thiophenes/chemistry , Thiophenes/radiation effects , Ultraviolet Rays , Aziridines/chemical synthesis , Aziridines/chemistry , Aziridines/radiation effects , Imines/chemical synthesis , Imines/chemistry , Molecular Structure , Phosphoranes/chemical synthesis , Phosphoranes/chemistry , Phosphoranes/radiation effects , Photochemistry , Photolysis , Stereoisomerism
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