<i>N</i><sup>α</sup>-arylsulfonyl histamines as selective β-glucosidase inhibitors
作者:M. O. Salazar、M. I. Osella、I. A. Ramallo、R. L. E. Furlan
DOI:10.1039/c8ra06625f
日期:——
A selective β-glucosidase inhibitor was discovered using the chemically engineered extracts approach.
使用化学工程提取方法发现了一种选择性β-葡萄糖苷酶抑制剂。
US6080871A
申请人:——
公开号:US6080871A
公开(公告)日:2000-06-27
Palladium catalysed tandem cyclisation–anion capture. Part 7: Synthesis of derivatives of α-amino esters, nitrogen heterocycles and β-aryl/heteroaryl ethylamines via in situ generated vinylstannanes
作者:Adele Casaschi、Ronald Grigg、J.M Sansano
DOI:10.1016/s0040-4020(00)01030-9
日期:2001.1
terminal alkynes containing a β-N atom affords mainly α-vinylstannanes which serve as anion capture agents in palladium catalysed cyclisation–anion capture processes leading to derivatives of α-amino esters, nitrogen heterocycles and β-aryl/heteroaryl ethylamines in good yield.