Title of article :
Convenient synthesis of 5-aryl(alkyl)sulfanyl-1,10-phenanthrolines from 5,6-epoxy-5,6-dihydro-1,10-phenanthroline, and their activity towards fungal β-d-glycosidases
Author/Authors :
Irina A. Dotsenko، نويسنده , , Matthew Curtis، نويسنده , , Nataliya M. Samoshina، نويسنده , , Vyacheslav V. Samoshin، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2011
Pages :
9
From page :
7470
To page :
7478
Abstract :
A broad series of novel 5-aryl(alkyl)sulfanyl-1,10-phenanthrolines has been prepared by a new simple procedure: a treatment of the commercially available 5,6-epoxy-5,6-dihydro-1,10-phenanthroline with various thiols in the presence of a base. Other functional groups attached to the thiol allow a use of the products as building blocks in synthesis of versatile ligands and in functionalization of surfaces. The synthesized phenanthrolines showed a moderate ability as activators or inhibitors of fungal β-d-glucosidases and β-d-galactosidases.
Keywords :
1 , 10-Phenanthroline , Epoxide deoxygenation , Base-induced aromatization , Glycosidase activators/inhibitors
Journal title :
Tetrahedron
Serial Year :
2011
Journal title :
Tetrahedron
Record number :
1103686
Link To Document :
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