𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis of α-d-C-glucoside employing dichloroketene cycloaddition and Baeyer-Villiger oxidation

✍ Scribed by Jonghoon Oh

Publisher
Elsevier Science
Year
1997
Tongue
French
Weight
98 KB
Volume
38
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Criegee rearrangement of α-alkoxy hydrop
Criegee rearrangement of α-alkoxy hydroperoxides a synthesis of esters and lactones that complements the baeyer-villiger oxidation of ketones
✍ Stuart L. Schreiber; Wai-Fong Liew 📂 Article 📅 1983 🏛 Elsevier Science 🌐 French ⚖ 212 KB

cr-Alkoxy hydroperoxides undergo Criegee rearrangment upon treatment with (CH,CO),O to provide esters or lactones. The acylation of hydroperoxides results in the formation of peroxyesters which can undergo the Criegee rearrangement to afford ketones or ketals.' We have studied the acylation of an a-