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Synthesis of Tetrahydropyridoimidazole-2-acetates: Effect of Carboxy and Methoxycarbonyl Groups at C(2) on the Inhibition of Some β- and α-Glycosidases.

✍ Scribed by Miroslav Terinek; Andrea Vasella

Book ID
101970614
Publisher
John Wiley and Sons
Year
2005
Weight
14 KB
Volume
36
Category
Article
ISSN
0931-7597

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Synthesis of Tetrahydropyridoimidazole-2
Synthesis of Tetrahydropyridoimidazole-2-acetates: Effect of Carboxy and Methoxycarbonyl Groups at C(2) on the Inhibition of Some β- and α-Glycosidases
✍ Miroslav Terinek; Andrea Vasella 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 German ⚖ 157 KB

## Abstract The __gluco__‐ and __manno__‐tetrahydropyridoimidazole‐2‐acetates and ‐acetic acids **16** and **17**, and **20** and **21**, respectively, were synthesized by condensation, in the presence of HgCl~2~, of the known thionolactam **26** with the __β__‐amino ester **25** that was obtained