Synthesis of Novel Cyclopropyl Nucleoside Analogues as Potential Antiherpetic Agent
نویسندگان
چکیده
منابع مشابه
Combinatorial synthesis of galactosyl-1,3,5-triazines as novel nucleoside analogues.
Herein we report a parallel solid-phase synthesis of 1,3,5-triazine based nucleoside analogues by a three-step substitution, starting from 2,4,6-trichloro-1,3,5-triazine. A library of 80 galactosyl-1,3,5-triazine compounds was prepared in high purity without extensive reaction conditions or tedious purification, suggesting the generality of this method.
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Rene Csuk, Anja Kern, and Kristina Mohr Institut für Organische Chemie. Martin-Luther-Universität Halle-Wittenberg, Kurt-Mothes-Str. 2, D-06120 Halle (Saale), Germany Reprint requests to Prof. Dr. R. Csuk. E-mail: [email protected] Z. Naturforsch. 54b, 1463-1468 (1999); received July 9, 1999 Nucleoside Analogues, HPLC A novel class of nucleoside analogues containing adenine, uracil, thym...
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Ursolic acid (UA) is a naturally bioactive compound that possesses potential anti-diabetic activity. The relatively safe and effective molecule intrigued us to further explore and to improve its anti-diabetic activity. In the present study, a series of novel UA analogues was synthesized and their structures were characterized. Their bioactivities against the α-glucosidase from baker's yeast wer...
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ژورنال
عنوان ژورنال: Nucleic Acids Symposium Series
سال: 2008
ISSN: 0261-3166,1746-8272
DOI: 10.1093/nass/nrn310