作者:Wei Li、Shridhar Bhat、Jun O. Liu
DOI:10.1016/j.tetlet.2011.07.094
日期:2011.9
A simple and highly efficient route to the FKBP-binding domain (FKBD) from the natural product rapamycin has been developed, which entails a sequence of ozonolysis/Baeyer-Villiger/Wittig reactions. The newly synthesized FKBD may serve as a core to assemble hybrid macrocyclic libraries for the discovery of novel probes of protein function and to synthesize new ligands for the FKBP family of proteins. (C) 2011 Elsevier Ltd. All rights reserved.