244282-22-2Relevant academic research and scientific papers
N-Iodosuccinimide-mediated intramolecular aglycon delivery
Ennis,Fairbanks,Slinn,Tennant-Eyles,Yeates
, p. 4221 - 4230 (2007/10/03)
Enol ethers may be accessed via Tebbe methylenation of either 2-O acetates or para-methoxybenzoates. N-Iodosuccinimide may then be employed to achieve both tethering and thioglycoside activation allowing the stereoselective synthesis of α-glucosides and β-mannosides, either in a one or two step procedure.
Stereoselective synthesis of α-glucosides and β-mannosides: Tethering and activation with W-iodosuccinimide
Ennis
, p. 1387 - 1390 (2007/10/03)
The stereoselective synthesis of both a-glucosides and β-mannosides may be readily achieved by the use of AModosuccinimde, both to effect mixed ketal formation and subsequent intramolecular aglycon delivery (IAD). Thieme Stuttgart.
