当前位置: X-MOL 学术Carbohydr. Res. › 论文详情
Our official English website, www.x-mol.net, welcomes your feedback! (Note: you will need to create a separate account there.)
An expedient synthesis of benzyl 2,3,4-tri-O-benzyl-β-d-glucopyranoside and benzyl 2,3,4-tri-O-benzyl-β-d-mannopyranoside
Carbohydrate Research ( IF 2.4 ) Pub Date : 2005-05-01 , DOI: 10.1016/j.carres.2005.02.013
Wallach Lu , Latifeh Navidpour , Scott D. Taylor

An efficient three-step synthesis of benzyl 2,3,4-tri-O-benzyl-beta-D-glucopyranoside, a widely used building block in carbohydrate chemistry, is described. The key step is the selective debenzylation-acetylation of perbenzylated beta-glucose using ZnCl2-Ac2O-HOAc. This approach was also used to affect an efficient three-step synthesis of benzyl 2,3,4-tri-O-benzyl-beta-D-mannopyranoside.

中文翻译:

方便合成苄基2,3,4-三-O-苄基-β-d-吡喃葡萄糖苷和苄基2,3,4-三-O-苄基-β-d-甘露吡喃糖苷

描述了一种高效的三步合成苄基2,3,4-三-O-苄基-β-D-吡喃葡萄糖苷,它是碳水化合物化学中广泛使用的组成部分。关键步骤是使用ZnCl2-Ac2O-HOAc对过苄基化的β-葡萄糖进行选择性脱苄基化-乙酰化。该方法也用于影响苄基2,3,4-三-O-苄基-β-D-甘露吡喃糖苷的有效三步合成。
更新日期:2005-05-01
down
wechat
bug