supported by the National Natural Science Foundation of China (Nos. 22171220);the Fundamental Research Funds of the Central Universities (No. xtr072022003)。
A regioselective C-C bond cleavage/aminocarbonylation cascade is presented. In recent years, tremendous progress has been made in the alkoxyl radical-mediated C-C bond cleavage of unstrained monocarbocycles. In contra...
the National Natural Science Foundation of China(grant no.22271251);the Fundamental Research Funds for the Central Universities(grant nos.226-2023-00016,226-2023-00115,and 226-2022-00224).
In sharp contrast to the well researched and well developed aminocarbonylation of alkenes,the dearomative carbamoylation of abundant areneπ-systems has scarcely been studied despite its great potential to enrich the ...
The National Key Research and Development Program of Ministry of Science and Technology(No.2022YFA1504602);Natural Science Foundation of Jiangsu Province(No.BK20211094);National Natural Science Foundation of China(No.22302214,21972152,U22B20137).
Carbonylation reactions,crucial for carbonyl group incorporation,struggle with the inherent complexity of achieving selective mono-or double-carbonylation on single substrates,often due to competing reaction pathways....
Financial support from the National Natural Science Foundation of China(Nos.21971201,22171220);the Fundamental Research Funds of the Central Universities(No.xtr072022003)。
A photoinduced copper-catalyzed alkoxyl triggered C-C bond cleavage/aminocarbonylation cascade is presented.Through adjusting the structure of alkoxyl radical precursors,functionalized lactones and ketoamides were syn...
the financial support from the National Natural Science Foundation of China(21971081,22171099,21820102003,91956201,22203034,and 92256301);the Double-Thousand Talents Plan of Jiangxi Province(jxsq2023102004);the Open Research Fund of School of Chemistry and Chemical Engineering,Henan Normal University(2021YB02);and the Program of Introducing Talents of Discipline to Universities of China(111 Program,B17019).
Catalytic four-component radical carbonylation of unactivated alkenes has recently been recognized as a robust protocol for rapid construction of various structurally diverse carbonyl compounds.Given the significance ...
supported by the National Key R&D Program of China(2021YFA1501100);the National Natural Science Foundation of China(22005007);the New Cornerstone Science Foundation,and Liaoning Binhai Laboratory Project(LBLF-202306);the Tencent Foundation through the XPLORER PRIZE.
A hydrogen storage system was developed via heterogeneous catalysis,employing the dehydrogenative coupling of methanol and N,N′-dimethylethylenediamine to efficiently produce high-purity H_(2).In this process,the Cu/...
financial supports from the National Natural Science Foundation of China(Nos.21772035,22022204,22072167,21202206);Natural Science Foundation of Hunan Province(Nos.2021JJ40147)。
α,β-Unsaturated primary amides are important intermediates and building blocks in organic synthesis.Herein,we report a ligand-free iron-catalyzed hydroaminocarbonylation of alkynes using NH_(4)HCO_(3)as the ammonia ...
We gratefully acknowledge the National Natural Science Foundation of China(21772198,21871268,22071250);the Frontier Research Program of Bioland Laboratory(Guangzhou Regenerative Medicine and Health Guangdong Laboratory)(2018GRZ110105017);the Natural Science Foundation of Guangdong Province of China(2020A1515011428);the“BAGUI Scholar”Program of Guangxi Province of China for financial support and Prof.Wenjun Tang at Shanghai institute of Organic Chemistry for providing some of ligands for free.
An unprecedented tandem carbonylation/aminocarbonylation triggered by palladium-catalyzed enantio-selective Heck-type exocyclopalladation delivering chiral heterocyclicα-ketoamides has been developed.The uncommon dou...
An efficient route for the palladium-catalyzed reductive aminocarbonylation of olefins with nitroarenes was developed using carbon monoxide(CO)as both reductant and carbonyl source,which enables facile access to amide...