Grants from the National Natural Science Foundation of China(22271077,21925103,21901062);the Natural Science Foundation of Henan(232300421078,222301420046);the Program for Science&Technology Innovation Talents in Universities of Henan Province(24HASTIT001);the China Postdoctoral Science Foundation(2021M690890);Henan University are gratefully acknowledged.
α-Azaarene quaternary carbon centers are prevalent in drug molecules,making the development of efficient synthetic approaches of great interest.Herein,we describe an unprecedented method for constructingα-all-carbon...
supported by the National Natural Science Foundation of China(22171072,21925103,22301061);Henan Normal University。
Direct enantioselective reduction of the C=C bond ofβ-polyfluoro-alkylated enones is an important but long-pending subject in asymmetric catalysis.Here,we report on the viability of visible light-driven cooperative p...
supported by the Dalian Institute of Chemical Physics,the Chinese Academy of Sciences;the National Natural Science Foundation of China(21472186,21272231)。
A nickel-hydride(Ni H)-catalyzed migratory and nonmigratory hydroalkylation reaction of 2-alkenyl azaarenes with alkyl iodines has been established through strategic modulation of N-or P-donor ligands.This method enab...
supported by Natural Science Foundation of Heilongjiang Youth Fund (No. YQ2021B002);Heilongjiang Postdoctoral Scientific Research Developmental Fund (No. LBH-Q20018);State Key Laboratory of Urban Water Resource and Environment (Harbin Institute of Technology)。
A novel air-stable n-type benzothiaphene endcapped azaarene(BTPQ) and its sulfonated derivative(BSPQ) were prepared via two pathways and characterized by NMR, UV–vis, fluorescence and cyclic voltammetry spectroscopy....
The development of catalytic asymmetric radical reactions is an attractive but formidable task.The high reactivity of radicals enables the use of readily accessible feedstocks and mild reaction conditions,but it leads...
This work was supported by the National Natural Science Foundation of China(21702091);Science and Technology Innovation Development Plan of Yantai(2020MSGY114);Yantai“Double Hundred Plan”;The authors also thank the Talent Induction Program for Youth Innovation Teams in Colleges and Universities of Shandong Province;The Graduate Innovation Foundation of Yantai University(YDYB2128)is gratefully acknowledged(for Y.-J.Hu).
An I_(2)-mediated[3+2]annulation of methyl-azaarenes with alkyl_(2)-isocyanoacetates or amino acid ester hydrochlorides has been demonstrated.This strategy involves CuN bond cleavage of isocyanides and can selectively...
Cooperative hydrogen atom transfer and chiral hydrogen‐bonding catalysis as a new platform for the asymmetric synthesis of azaarene derivatives is reported.By using a tetrabutylammonium decatungstate as the photocata...
This work was supported by the National Natural Science Foundation of China(21702091);the Science and Technology Innovation Development Plan of Yantai(2020MSGY114);the Yantai“Double Hundred Plan”.
A high-efficiency strategy for the synthesis of furoxans and 1,2,4-oxadiazoles has been developed,using tert-butyl nitrite(TBN)as the nitrogen source.Azaarene nitrile oxides as activated intermediates were generated i...
supported by the National Natural Science Foundation of China(21925103,21901062);Key Technologies R&D Program of Henan(202102310005);Henan Normal University;Henan University。
The first enantioselective Beckwith-Enholm cyclization reaction is reported herein.Under cooperative photoredox and chiral hydrogen-bonding catalysis mediated by visible light,cyclization of carbonyls with azaarene-ba...
Financial support from the National Natural Science Foundation of China(No.21402103);the research fund of Qingdao Agricultural University's High-level Person(No.631303);the Scientific Research Foundation of Shandong Province Outstanding Young Scientist Award(No.BS2013YY024) were gratefully acknowledged
A method of C(sp^3)-H bond functionalization of methyl azaarenes catalyzed by alumina-supported heteropoly acid and addition to isatins was developed. This transformation could be used for the synthesis of biologica...