𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Kinetics and mechanism of hydrolysis of 1-(2′-acetoxybenzoyl)-2-deoxy-α-D-glucopyranose, a novel aspirin prodrug

✍ Scribed by Anwar Hussain; J. Truelove; H. Kostenbauder


Publisher
John Wiley and Sons
Year
1979
Tongue
English
Weight
276 KB
Volume
68
Category
Article
ISSN
0022-3549

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


A convenient synthesis of 2-deoxy-2-[(R)
✍ Ingolf Macher 📂 Article 📅 1987 🏛 Elsevier Science 🌐 English ⚖ 417 KB

The crystalline tris(hydroxymethyl)ainomethane ("Tris") salt of 2-deoxy-2-[(R)-3-hydroxytetradecanamido]-3-0-[(R)-3-hydroxytetradecanoyl]-cY-D-glucopyranose 1 -phosphate (lipid X) has been synthesised from 2-animo-2-deoxy-D-glucose hydrochloride in five steps in -50% overall yield. The key step was

Kinetics and mechanism of hydrolysis of
✍ Yoke-Leng Sim; Emmy Fadhiza Damit; Azhar Ariffin; M. Niyaz Khan 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 160 KB

## Abstract A kinetic study on hydrolysis of N‐(2′‐hydroxyphenyl)phthalamic acid (**1**), N‐(2′‐methoxyphenyl)phthalamic acid (**2**), and N‐(2′‐methoxyphenyl)benzamide (**3**) under a highly alkaline medium gives second‐order rate constants, __k__~OH~, for the reactions of HO^−^ with **1, 2**, and

Synthesis and Evaluation of N-Acetyl-2-a
✍ Roshini Rajan; Thresen Mathew; Radovan Buffa; Frédéric Bornancin; Marco Cavallar 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 German ⚖ 274 KB

## Abstract magnified image The __N__‐acetyl‐2‐amino‐2‐deoxy‐__α__‐D‐galactopyranosyl 1‐thio‐7‐oxaceramide **1** was synthesized by substituting the 7‐oxasphingosine triflate **3** with __α__‐D‐__N__‐acetyl‐1‐thiogalactosamine (**2**). The triflate **3** was obtained from azide **4**. Thiol **2**

Synthesis, Crystal Structure and Hydroly
✍ Jingyu Zhang; Xuehui Hou; Hongmin Liu 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 204 KB

## Abstract A novel anhydrogalactosucrose derivative 2′‐methoxyl‐__O__‐1′,4′:3′,6′‐dianhydro‐__β__‐__D__‐fructofuranosyl 3,6‐anhydro‐4‐chloro‐4‐deoxy‐__α__‐__D__‐galactopyranoside (**4**) was prepared from 3,6:1′,4′:3′,6′‐trianhydro‐4‐chloro‐4‐deoxy‐galactosucrose (**3**) via a facile method and ch