摘要
在K_2CO_3和相转移催化剂TBAB存在下,氨基酸酯与手性源(R)-5-(l-氧基)-2(5H)-呋喃酮于室温下反应,得到一系列具有氨基酸结构组分的手性γ-丁内酯化合物。所有合成化合物的结构通过红外、核磁共振、高分辨质谱等进行了确认,并通过底物结构、反应规律以及产物的核磁共振氢谱分析,确认了新形成手性中心的绝对构型。
A series of chiral γ-butyrolactones containing amino acid building block were synthesized via the reaction of amino acid ester with chiral synthon( R)-5-( l-menthnol)-2( 5H)-furanone in the presence of K_2CO_3 and phase transfer catalysis TBAB at room temperature. All the products were confirmed by IR,~1HNMR,^(13)CNMR,and HR-MS,and the absolute configuration of the stereogenic center was confirmed through the structure of the substrate,reaction regularity and ~1HNMR analysis.
出处
《化学试剂》
CAS
北大核心
2016年第3期203-206,共4页
Chemical Reagents
基金
河南省2012年科技发展计划资助项目(1223-00410265)
关键词
手性
合成
氨基酸
Γ-丁内酯
chirality
synthesis
amino acid
γ-butyrolactone