期刊
JOURNAL OF ORGANIC CHEMISTRY
卷 78, 期 20, 页码 10395-10404出版社
AMER CHEMICAL SOC
DOI: 10.1021/jo401801j
关键词
-
资金
- National Research Foundation of Korea (NRF)
- Ministry of Education, Science and Technology [2012M3A7B4049656]
- National Research Foundation of Korea [2012M3A7B4049656] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
A highly efficient [4 + 2] annulation route to polysubstituted indolizines is described employing a domino Knoevenagel condensation/intramolecular aldol cyclization process as a key step. Construction of pyridine rings in indolizine skeleton was rapidly achieved from several pyrrole-2-carboxaldehydes in good to excellent yields, leading to indolizines with various substituents at the 5, 6, and 7 positions depending on the reacting active methylene partners.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据