化学
糖基
糖基化
糖化学
糖苷键
另一个
亚砜
反应性(心理学)
糖基供体
试剂
组合化学
N-连接糖基化
碳水化合物合成
糖苷
立体化学
亲核细胞
碳水化合物
有机化学
生物化学
酶
替代医学
病理
医学
作者
Jing Zeng,Yan Liu,Wei Chen,Xin Zhao,Lingkui Meng,Qian Wan
标识
DOI:10.1007/s41061-018-0205-4
摘要
Carbohydrate chemistry has benefited a lot from the intrinsic reactivity of sulfoxide since it was introduced in glycosylation reactions by Kahne in 1989. Since then, extensive studies have been explored by employing sulfoxide as glycosyl donors and activation reagents in construction of glycosidic bonds. As glycosyl donors, the sulfinyl groups could locate either directly or remotely at anomeric position. This chapter focuses on the establishment and development of sulfoxides as glycosyl donors in glycosylation reactions, with an emphasis on their applications and postulated mechanisms.
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