𝔖 Bobbio Scriptorium
✦   LIBER   ✦

New 4-Amino-2-azabicyclo[3.2.2]nonane Derivatives and Their Antiprotozoal Potencies.

✍ Scribed by Werner Seebacher; Marcel Kaiser; Reto Brun; Robert Saf; Robert Weis

Publisher
John Wiley and Sons
Year
2007
Weight
24 KB
Volume
38
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis of 2-Azabicyclo[3.2.2]nonane-D
Synthesis of 2-Azabicyclo[3.2.2]nonane-Derived Monosaccharide Mimics and Their Evaluation as Glycosidase Inhibitors
✍ Stephan Buser; Andrea Vasella 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 German ⚖ 143 KB 👁 1 views

The racemic 2-azabicyclo[3.2.2]nonanes 5 and 18 were synthesized and tested as b-glycosidase inhibitors. The intramolecular Diels-Alder reaction of the masked o-benzoquinone generated from 2-(allyloxy)phenol ( 6) gave the a-keto acetal 7 which was reduced with SmI 2 to the hydroxy ketone 8. Dihydrox

4-Oxa(thia)-9-oxa-2-azabicyclo[4.2.1]non
4-Oxa(thia)-9-oxa-2-azabicyclo[4.2.1]nonane-3-on(thion) derivatives
✍ Vinko Škarić; Marijan Hohnjec; Djurdjica Škarić 📂 Article 📅 1976 🏛 John Wiley and Sons 🌐 German ⚖ 484 KB

## Abstract The synthesis of 7,8‐dihydroxy‐2‐(2‐methoxycarbonylethyl)‐4,9‐dioxa‐2‐azabicyclo[4.2.1]nonane‐ 3‐thione (**16**) and of its parents 9‐oxa‐4‐thia‐3‐thione **17**, and 9‐oxa‐4‐thia‐3‐one **18** is described. The conversion of 5′‐deoxy‐5′‐iodo‐2′,3′‐__O, O__‐isopropylidene‐5,6‐dihydrouridi