the National Natural Science Foundation of China(Nos.21672199,21790333,21925111 and 21702197);the Fundamental Research Funds for the Central Universities(No.WK2060190086).
Main observation and conclusion A new strategy for the generation of the active Pd-alkyl species from aminal via C-N bond activation has been established,in which the formation of zwitterionic intermediate through aza...
This research was supported by the National Natural Science Foundation of China(Nos.21925111,21672199,21790333,and 21702197);the Fundamental Resedrch Funds for the Central Universities(No.WK2060190086).
Summary of main observation and conclusion A new and eficient cyclization reaction has bleen developed to synthesize cyclic a,a-disubstituted B-amino esters via iron-catalyzed intramolecular aminomethyloxygenative cyc...
the National Natural Science Foundation of China (Nos. 21502098, 21672105);the Natural Science Foundation of Tianjin (17JCYBJC19700);the Qindao National Laboratory for Marine Scie nee and Tech no logy, and the State Key Laboratory of Elemento-Organic Chemistry at Nankai University for financial support of this work.
Summary of main observation and conclusion A 4+2 cycloaddition reaction of NH-free benzazetidines with indoles under the catalysis of camphorsulfonic acid was developed. This method shows a broad substrate scope of be...
This research was supported by the National Natural Science Foundation of China (Nos. 21672199 and 21790333) and CAS Interdisciplinary Innovation Team.
A new palladium-catalyzed selective aminomethylation of conjugated 1,3-dienes with aminais via double C-N bond activation is described. This simple method provides an effective and rapid approach for the synthesis of ...