A concise synthesis of HIV integrase inhibitors bearing the dipyridone acid motif
Tetrahedron Letters(2011)
摘要
An efficient route to dipyridone acid HIV integrase inhibitors is developed. The key steps include a one-pot three-step formation of the core template (containing one point of structural diversity) followed by a regioselective benzylation and in situ deprotection to afford the title compounds.
更多查看译文
关键词
Dipyridone acid,Integrase,Heterocycles,Antiviral agents,Ring-closure
AI 理解论文
溯源树
样例
生成溯源树,研究论文发展脉络
Chat Paper
正在生成论文摘要