Synthesis of N-Propargyl Iminosugar Scaffolds for Compound Library Generation using Click Chemistry
作者:Brendan L. Wilkinson、Laurent F. Bornaghi、Marie Lopez、Peter C. Healy、Sally-Ann Poulsen、Todd A. Houston
DOI:10.1071/ch09426
日期:——
We have developed an efficient synthesis of N-propargyl iminosugars for use in diversity-oriented library development. Through a common, crystalline intermediate both piperidine and azepane scaffolds can be prepared with an alkyne functional group, allowing for further elaboration through reaction with azides.
我们已经开发了一种N-炔丙基亚氨基糖的有效合成方法,可用于面向多样性的文库开发。通过普通的结晶中间体,哌啶和氮杂环丙烷支架都可以制备成具有炔烃官能团,从而可以通过与叠氮化物的反应进行进一步的精制。