硫脲
角鲨胺
立体选择性
化学
糖基
糖基化
亲核细胞
有机催化
对映选择合成
催化作用
有机化学
组合化学
药物化学
立体化学
生物化学
作者
Márcia Rénio,M. Rita Ventura
标识
DOI:10.1002/cctc.202401227
摘要
Abstract Two new mono‐thiourea, four bis‐thiourea and one squaramide organocatalysts were synthesised from L‐tartaric acid. These organocatalysts were able to activate glycosyl phosphates for stereoselective nucleophilic substitution reactions with broad functional group compatibility under mild conditions. The influence of the number and position of the thiourea groups and the proximity of the asymmetric centre to the catalytic important atoms for the stereoselective outcome of the glycosylation reactions was studied. 1,2‐ cis Glycosides were obtained in up to 85 % yield and high diastereoselectivity (up to α:β 83 : 17).
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