the financial support from the National Natural Science Foundation of China(Nos.21971224,22171249);the Natural Science Foundation of Henan Provinee,China(No.202300410375);the College Students'Innovation and Entre-preneurship Training Program of Zhengzhou University(No.2021cxcy197).
An efficient and eco-friendly carbon nitride nanosheet(NM-g-C3N4)-catalyzed decarboxylative coupling reaction of imidazo-fused heterocycles(i.e.,imidazo[1,2-a]pyridines,benzo[d]imidazo[2,1-b]thiazole)with N-phenylglyc...
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...
We are grateful for the financial support from the National Basic Research Program of China(No.(973J-2015CB856603);the Strategic Priority Research Program of the Chinese Academy of Sciences(No.XDB20000000);sioczz201808,the National Natural Science Foundation of China(Nos.21421091,21372250,21121062,21302203,20732008,21772037,21772226,21861132014,and 91956115).
Summary of main observation and conclusion A Rh^Ⅲ/Ag^Ⅰrelay-catalyzed C(sp^2)—H coupling of indoles with triarylhexahydrotriazine(THT)is reported in this context.Upon merging Rh^Ⅲ-catalyzed C(sp^2)—H bond activat...
This work was supported by the Ministry of Education(MOE)of Singapore(no.R-143-000-A93-112).
Chiral amines are synthetically versatile intermedi-ates used for the preparation of a wide range of biologically active compounds and drugs.Compared with the well-developed synthesis ofα-stereogenic amines,the estab...
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 ...
This work was financially supported by the Natural Science Foundation of Tianjin (No. 013606111)
The regioselective Mannich-type aminomethylation of hydroquinone afforded a nitrogen-containing compound, 2,5-bis-(morpholinomethyl)hydroquinone A, and its crystal structure was determined by single-crystal X-ray di...