Morita–Baylis–Hillman adducts as building blocks of heterocycles: a simple approach to 4-substituted pyrazolones, and mechanism investigation via ESI–MS(/MS)
摘要:
We describe herein an efficient approach for the preparation of 4-substituted 2,3-dihydro-1H-pyrazol-3-ones starting from Morita-Baylis-Hillman adducts. These heterocycles were obtained in two or three steps as single isomers with moderate to good overall yields. One efficient and alternative methodology for the synthesis of alpha-methyl-beta-ketoesters is also reported (up to 91 % yield). Additionally, the mechanism of formation of pyrazolones was investigated employing ESI-MS/MS reaction monitoring.
作者:Zhenhua Zhang、Yiyang Liu、Mingxing Gong、Xiaokun Zhao、Yan Zhang、Jianbo Wang
DOI:10.1002/anie.200906349
日期:2010.2.1
On the move: A palladium‐catalyzed reaction of aryl iodides, diazo compounds or N‐tosylhydrazones, and carbon monoxide affords β‐oxo esters or ketones/enones (see scheme; DCE=1,2‐dichloroethane). The products are delivered with high efficiency through the title sequence.
RIBOSOME-MEDIATED INCORPORATION OF PEPTIDES AND PEPTIDOMIMETICS
申请人:Arizona Board of Regents on Behalf of Arizona State University
公开号:US20180002709A1
公开(公告)日:2018-01-04
Modified ribosomes that were selected using a dipeptidyl-puromycin aminonucleoside are used to mediate site-specific incorporation of one or more peptides and peptidomimetics into protein in a cell free translation system. In addition, new fluorescent dipeptidomimetics have been synthesized and incorporated into proteins, as well as modified proteins containing one or more non-naturally occurring dipeptides.