supported by the National Natural Science Foundation of China(22101261);the Natural Science Foundation of Henan Province(232300421087,232301420045);the Zhengzhou University of China(2023ZZUJGXM168).
A novel method for synthesizingα-oxygen organoboron compounds has been developed through acylsilane-based carbene insertion reactions into C—B bonds.As coupling partners,readily available organoboron compounds(alken...
supported by the National Key R&D Program of China (2022YFA1506100);the National Natural Science Foundation of China (21901191);the Fundamental Research Funds for the Central Universities (2042023kf0202);the China Postdoctoral Science Foundation (2023TQ0250)。
Previous carbene insertion to C–H bonds of 1,3-azoles relied on metal carbene species. Herein, we report a metal-free C(sp^(2))–H bond functionalization of 1,3-azoles with trifluoroacetylsilanes. The reaction featur...
supported by the National Natural Science Foundation of China(22331004,22125108 and 22121001);the National Fund for Fostering Talents of Basic Science NFFTBS(J1310024)。
α-Imino metal carbenes are versatile intermediates in organic synthesis,and have broad applications in the assembly of divergent N-heterocycles.However,the catalytic enantioselective desymmetrization based onα-imino...
The National Natural Science Foundation of China(22078317)。
Efficient use of energy is a pressing issue.Improvement of chemical processes is currently an important target for energy efficiency.Although chemical processes are independent of pathways with respect to the final en...
the National Natural Science Foundation of China(nos.21625204 and 21971119);the“111”project(B06005)of the Ministry of Education of China;National Program for Support of Top-notch Young Professionals;Key-Area Research and Development Program of Guangdong Province(no.2020B010188001)for financial support.
Since organoboron compounds readily undergo a diverse array of transformations and are widely used in various fields,the development of C-B-bondforming reactions have attracted considerable attention.Herein,we report ...
the National Natural Science Foundation of China(No.21901057);the Anhui Provincial Natural Science Foundation(No.1908085QB62);the Fundamental Research Funds for the Central Universities of China(No.PA2020GDSK0070);the National Natural Science Foundation of China(No.51803045).
Ring-opening metathesis polymerization(ROMP)of norbornene by binuclear vanadium alkylidene in-situ formed from dialkyl complexes was investigated.Higher activities were observed by the binuclear system than mononuclea...
supported by National Natural Science Foundation of China(no.21901259);Guangdong Basic and Applied Basic Research Foundation(no.2020A1515011116);the Program for Guangdong Introducing Innovative and Entrepreneurial Teams(no.2016ZT06Y337);the National Science&Technology Major Project“Key New Drug Creation and Manufacturing Program”of China(no.2018ZX09711002-006).
Enantioenrichedγ-butenolides are valuable structural cores in many pharmaceuticals and natural products,but their direct and catalytically asymmetric assembly remains rare.Here,we report an efficient,atom-economic sy...
supported by the National Natural Science Foundation of China(No.21403221 and No.91441106)
The formation of the aromatic ring during the formation of polycyclic aromatic hydrocarbons (PAHs) remains controversial and the experimental evidence is still lacking. Moreover, the formation mechanism of benzene fro...
A straightforward and efficient protocol for dearomatizing indoles is described.The reaction,catalyzed by an inexpensive Co(III)/Zn(II)catalyst,starts from easily accessible N‐pyrimidinyl indoles and ene‐yne ketones...
The project is supported by the National Basic Research Pro- gram of China (973 Program, No. 2015CB856600) and the Natio- anal Natural Science Foundation of China (Grant 21332002, 21472004).
The palladium(o)-catalyzed nitrogen insertion into cyclic Si-Si bonds has been realized by using N-tosylhydrazones/diazo compounds as the nitrogen source. The palladium(Ⅱ) nitrene formation and subsequent migrato...