为发展新的手性配体,降低手性配体的合成成本,检验由芳醛与手性氨基酸酯缩合还原反应的普适性,以L-丝氨酸为手性源,经酯化,缩合,还原氨化,关环等反应,设计合成了一种新的茚满基氮杂环丙基二环丙基三级醇手性配体,其结构通过IR,1 H NMR,13 C NMR, HRMS进行了表征,发展了一条高效便捷合成这类具有光学活性化合物的方法。
A novel Indancarbaldehyde chiral β-amino alcohol ligand has been successfully synthesized from readily available L -methionine through esterification , condensation , reductive alkylation , and further treatment with RMgX.This synthesis method is convenient and practical , which can be applied to industrialization .The structures of the target compound and the intermediates were confirmed by IR ,1 H NMR,13 C NMR, HRMS.