Novel 1,2,4-triazine-quinoline hybrids: The privileged scaffolds as potent multi-target inhibitors of LPS-induced inflammatory response via dual COX-2 and 15-LOX inhibition
Novel 1,2,4-triazine-quinoline hybrids: The privileged scaffolds as potent multi-target inhibitors of LPS-induced inflammatory response via dual COX-2 and 15-LOX inhibition
An improved direct synthetic approach to anhydronucleosides
作者:Ibtehal A. Al-Juwaiser、Maher R. Ibrahim、Nouria A. Al-Awadi、Yehia A. Ibrahim
DOI:10.1016/j.tet.2008.06.016
日期:2008.8
The synthesis of anhydrothioglycosyls has been improved by studying the reaction under a variety of reaction conditions including gas phase pyrolysis, heating in a solvent of high boiling point, in the presence of different bases including triethylamine, DABCO, and DBU, and in a microwave reactor. (C) 2008 Published by Elsevier Ltd.