化学
催化作用
对映选择合成
烷基化
筑地反应
不对称氢化
有机化学
盐(化学)
药物化学
立体中心
作者
Ju-Song Yang,Ka Lu,Chen-Xiao Li,Zu-Hang Zhao,Xiao-Ming Zhang,Fu-Min Zhang,Yong-Qiang Tu
标识
DOI:10.1002/anie.202114129
摘要
Novel asymmetric mono- and dialkylation reactions of α-substituted 2,5-diketopiperazines catalyzed by new chiral spirocyclic-amide-derived triazolium organocatalysts have been developed, resulting in a range of enantioenriched 2,5-diketopiperazine derivatives containing one or two tetrasubstituted carbon stereocenters. The reactions feature high yields (up to 98%), and excellent cis-diastereo- and enantioselectivities (up to >20:1 dr, >99 % ee), and they provide a new asymmetric synthetic approach to important functionalized 2,5-diketopiperazine skeletons. Furthermore, a possible reaction mechanism was proposed based on both control experiments and extensive DFT calculations.
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