Gati Wafa, Yamamoto Hisashi
Molecular Catalyst Research Center , Chubu University , 1200 Matsumoto-cho , Kasugai , Aichi 487-8501 , Japan . Email:
Chem Sci. 2016 Jan 1;7(1):394-399. doi: 10.1039/c5sc03307a. Epub 2015 Oct 6.
A highly diastereoselective approach for the synthesis of protected α,β-dioxyaldehydes derived from ()-tris(trimethylsilyl)silyl "super silyl" enol ethers is described. A general and highly -stereoselective aldol reaction directed by the "super silyl" group catalyzed by triflimide (HNTf) is developed providing α,β-dioxyaldehydes and 1,2,3-triol fragments which can be a useful platform for the elaboration of natural and unnatural sugar derivatives.
本文描述了一种从()-三(三甲基硅基)硅基“超级硅基”烯醇醚合成受保护的α,β-二氧醛的高非对映选择性方法。开发了一种由三氟甲磺酸亚胺(HNTf)催化的、由“超级硅基”基团导向的通用且高立体选择性的羟醛反应,可提供α,β-二氧醛和1,2,3-三醇片段,这些片段可为天然和非天然糖衍生物的合成提供有用的平台。