Department of Chemistry, Tufts University, 62 Talbot Ave., 02155, Medford, MA, USA.
Chem Rec. 2021 Nov;21(11):3102-3111. doi: 10.1002/tcr.202100141. Epub 2021 Jun 17.
While glycosyl triflates are frequently invoked as intermediates in many chemical glycosylation reactions, the chemistry of other glycosyl sulfonates remains comparatively underexplored. Given the reactivity of sulfonates can span several orders of magnitude, this represents an untapped resource for the development of stereoselective glycosylation reactions. This personal account describes our laboratories efforts to take advantage of this reactivity to develop β-specific glycosylation reactions. Initial investigations led to the development of 2-deoxy-sugar tosylates as highly selective donors for β-glycoside synthesis, an approach which has been used to great success by our group and others for the construction of deoxy-sugar oligosaccharides and natural products. Subsequent studies demonstrate that "matching" the reactivity of the sulfonate to that of the sugar donor leads to highly selective S 2-glycosylations with a range of substrates.
虽然糖基三氟甲磺酸酯经常被用作许多化学糖苷化反应的中间体,但其他糖基磺酸酯的化学性质仍相对未被充分探索。鉴于磺酸盐的反应性可以跨越几个数量级,这代表了开发立体选择性糖苷化反应的未开发资源。本个人述评描述了我们实验室利用这种反应性开发β-特异性糖苷化反应的努力。初步研究导致开发了 2-脱氧糖对甲苯磺酸酯作为β-糖苷合成的高选择性供体,我们小组和其他小组已成功地将该方法用于构建脱氧糖寡糖和天然产物。随后的研究表明,“匹配”磺酸盐的反应性与糖供体的反应性,可导致与一系列底物的高度选择性 S2-糖苷化。