grateful for financial support from the National Natural Science Foundation of China(grants 21722206,21672171);Financial support from the Scientific Fund of Northwest A&F University is also acknowledged.
Halocyclization of olefinic substrate enables the establishment of cyclic skeletons via intramolecular halonium-induced nucleophilic addition,which has been well utilized as a practical strategy for constructing cycli...
National Natural Science Foundation of China(No.21961015);the Natural Science Foundation of Jiangxi Province(No.20202ACBL203005)for financial support;the Open Project Program of Polymer Engineering Research Center,Jiangxi Science&Technology Normal University(No.KFGJ18014)。
We report a Pd-catalyzed halocyclization of unactivated 1,6-diynes with N-bromosuccinimide(NBS).This approach produces stereo-defined dibromo substituted dihydropyrans,tetrahydropyridines,and 3-methylene cyclohexenes ...
This work was supported by the National Natural Science Foundation of China(No.21520102003);the Hubei Province Natural Science Foundation of China(No,2017CFA010);The Pro-gram of Introducing Talents of Discipline to Universities of China(111 Program)is also appreciated.
Summary of main observation and conclusion Owing to the easy functionalization of 3-haloindolines to many biologically active compounds,extensive efforts have been made for their efficient preparation.Herein,an electr...
the University of Wisconsin-Madison and the American Chemical Society Petroleum Research Fund (48092-G) for funding
The discovery of the novel reactivity of conjugated enynes,mediated by readily available halogenation reagents,opens a broad range of mechanistically unique pathways for the synthesis of highly functionalized chiral a...