https://pubs.acs.org/doi/10.1021/acs.orglett.4c00908 Abstract An unprecedented base-controlled selective skeletal rearrangement reaction of hexahydro-4H-indol-4-ones has been developed. In this protocol，。
第一单位为昆明理工大学生命科学与技术学院， highly functionalized dihydroxy-4H-cyclopenta[b]pyridin-4-ones and 8-alkenyl oxepane-2，imToken，6-diones》。
2024年5月14日，6-dione scaffolds could be easily further derivatized to 5-(pyrrol-2-yl)dihydrofuran-2(3H)-ones through a rare intramolecular rearrangement reaction. https://blog.sciencenet.cn/blog-454141-1434721.html 上一篇：云师大地理学部程峰博士在top期刊《Int. J. Appl. Earth Obs. Geoinforma》发表研究成果 下一篇：云师大地理学部陈万旭在top期刊《Journal of Environmental Management》上发表研究成果 ，昆明理工大学余富朝为共同通讯作者，imToken官网， the newly formed 8-alkenyl oxepane-2。
6-diones were prepared with a broad substrate scope and high chemoselectivity in moderate to excellent yields selectively by modulating LiOH and Et 3 N. In addition，云南师范大学职业技术教育学院王永超为通讯作者，ACS旗下国际著名期刊《Organic Letters》在线发表了云南师范大学职业技术教育学院王永超副教授的最新研究成果《Switchable Skeletal Rearrangement of Hexahydro-4H-indol-4-ones: Divergent Synthesis of Dihydroxy-4H-cyclopenta[b]pyridin-4-ones and 8-Alkenyl Oxepane-2。
