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NUCLEOSIDES 5(15): SYNTHESIS OF NOVEL 1,2,4-TRIAZOLO[3,4-c]-1,2,4-TRIAZOLE NUCLEOSIDES
Journal article   Peer reviewed

NUCLEOSIDES 5(15): SYNTHESIS OF NOVEL 1,2,4-TRIAZOLO[3,4-c]-1,2,4-TRIAZOLE NUCLEOSIDES

M. A. N. Mosselhi and R. Neidlein
Nucleosides, nucleotides & nucleic acids, Vol.28(11-12), pp.1095-1103
11/2009
PMID: 20183576

Abstract

Biochemistry & Molecular Biology Life Sciences & Biomedicine Science & Technology
Ribosylation of 3-methylthio-5-phenyl-1,2,4-triazole (1) with ribose derivative 2 gave the protected 1,2,4-triazole-nucleoside 3, which reacted with hydrazine hydrate to afford the 3-hydrazino-1,2,4-triazole derivative 5. Reaction of 5 with aromatic aldehydes yielded the corresponding hydrazones 6, which cyclized under bromination in acetic acid to give 8. Debenzoylation of 8 afforded novel 1,2,4-triazolo[3,4-c]-1,2,4-triazole nucleosides 9.

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