Final Thoughts on Chemistry for 2,3,4,6-Tetra-o-acetyl-D-glucopyranose

If you are hungry for even more, make sure to check my other article about 10343-06-3. Synthetic Route of 10343-06-3

Synthetic Route of 10343-06-3. Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments.Introducing a new discovery about 10343-06-3, Name is 2,3,4,6-Tetra-o-acetyl-D-glucopyranose

An efficient and convenient synthetic route to glycosyl 1-beta-phosphates has been developed using diallyl chlorophosphate as a phosphorylating agent with 4-N,N-dimethylaminopyridine under mild conditions. Diallyl-glycosyl 1-beta-phosphate triesters of d-manno, l-glycero-d-manno-hepto-, d-gluco-, d-galacto-, and l-fuco-pyranose as well as lactose have been obtained by this strategy in good yields and excellent beta-selectivities. Furthermore, the diallyl 6-azido-mannosyl 1-beta-phosphate 2 was deprotected under mild conditions and converted into potentially clickable analogues of beta-mannosyl phosphoisoprenoids I and ADP-heptose II.

If you are hungry for even more, make sure to check my other article about 10343-06-3. Synthetic Route of 10343-06-3

Reference:
Tetrahydropyran – Wikipedia,
Tetrahydropyran – an overview | ScienceDirect Topics