An Efficient Assembly of Heterobenzazepine Ring Systems Utilizing an Intramolecular Palladium-Catalyzed Cycloamination
作者:Brandon J. Margolis、Jacob J. Swidorski、Bruce N. Rogers
DOI:10.1021/jo026546g
日期:2003.1.1
Azaheterocyclic compounds are interesting and medicinally relevant targets. Herein we disclose an improved synthesis into the oxazepine and thiazepine ring systems. The key step in the synthesis exploits recent advancements in the palladium-catalyzed amination reaction, which was utilized to form the seven-membered rings. General conditions for this reaction were Pd(2)dba(3), P(t-BU)(3), NaO-t-Bu alone or with K2CO3, in toluene. The scope of the reaction was investigated, and has been shown to be effective on a variety of substrates as illustrated.
Elaboration of the Oxazepine
Ring System via CuI/<scp>l</scp>-Proline-Catalyzed Intramolecular
Aryl Amination
作者:Dawei Ma、Lei Guo、Ben Li、Wenlong Huang、Gang Pei
DOI:10.1055/s-2008-1078506
日期:——
A two-step approach for assembling oxazepines is described, which started from 2-aminophenols and substituted 2-bromobenzyl bromides and used CuI/l-proline-catalyzed coupling reaction as the key step.