supported by the National Natural Science Foundation of China(No.22171046);the Hundred-Talent Project of Fujian(No.50021113).
The development of efficient and sustainable methods to obtain spirocyclic compounds is of significance as these structures are widely found in pharmaceuticals and agrochemicals.Herein,we disclose an electrochemical d...
the National Natural Science Foundation of China(22101075,U2004189);Central Plains Science and Technology Innovation Leader Project(224200510009);Postdoctoral Research Grant in Henan Province(202103085);Henan Key Laboratory of Organic Functional Molecules and Drug Innovation,and 111 Project(D17007)for financial support.
Herein,we report a condition-controlled divergent synthesis of spiro indene-2,1'-isoindolinones and spiro isochroman-3,1'-isoindolinones through cobalt-catalyzed formal[4+1]and[4+1+1]spirocyclization of aromatic amide...
We are grateful for the financial support from 111 Project(No.B18035)and“the Fundamental Research Funds for the Central Universities”.
Transition-metal-catalyzed cross-coupling reactions as very efficient and atom-economical approaches have been widely used to build up complex heterocyclic compounds.However,modification of 2-oxyl benzimidazole skelet...
We gratefully acknowledge the Provincial Planning Project of the Zhejiang Provincial Science and Technology Department(No.LGF19B060005)for financial support.
A novel and green route have been developed for the electrochemical synthesis of 3-halogenated spiro[4.5]trienones based on dearomative spirocyclization of alkynes with NaX(Br,I)as the halogen source.This transformati...
supported by the National Natural Science Foundation of China(21871094);the Guangxi Key Laboratory of Zhuang and Yao Ethnic Medicine[(2014)No.32];We also thank the support of the Hunan Provincial Key Laboratory of Materials Protection for Electric Power and Transportation(No.2021CL04).
Here is an operable and rare strategy for copper-initiated radical dearomative 2,5-alkylarylation of furan. By means of this strategy, we realized the dearomatization of furans to construct spirooxindoles with good yi...
This work is supported by the National Natural Science Foundation of China(Nos.22277110,81973177 and 31900875,China);the Natural Science Foundation of Henan Province(Nos.222300420069 and 222301420049,China);Program for Science&Technology Innovation Talents in Universities of Henan Province(No.21HASTIT045,China).
The design of new ligands with high affinity and specificity against the targets of interest has been a central focus in drug discovery.As one of the most commonly used methods in drug discovery,the cyclization repres...
the financial support from NSFC(grant nos.21871257,22022111,and 21801240);the Natural Science Foundation of Fujian Province(grant no.2020J02008);the Strategic Priority Research Program of the Chinese Academy of Sciences(grant no.XDB20000000).
Visible-light-induced reductive dearomatization of nonactivated arenes is a very challenging transformation and remains in its infancy.Herein,we report a novel strategy to achieve a visible-light-induced spirocyclizat...
the financial supports from the National Natural Science Foundation of China(Nos.22022111,21871257,21801240);the Natural Science Foundation of Fujian Province(No.2020J02008);the Strategic Priority Research Program of the Chinese Academy of Sciences(No.XDB20000000)。
A visible-light-induced spirocyclizative hydroarylation via reductive dearomatization of a series of non activated arenes including 2-phenyl indoles and naphthalene derivatives under mild conditions is de scribed.An i...
the National Natural Science Foundation of China(grant nos.21971204 and 21622203);the Innovation Capability Support Program of Shaanxi Province(grant no.2020TD-022).
A catalytic,enantioselective spirocyclization of formanilides or formylindolines and enamides has been developed herein.The reaction proceeds through a sequential iridium-catalyzed hydrosilylation of tertiary formanil...
financial support from Jiangsu Planned Projects for Postdoctoral Research Funds(No.2018K293C)。
A new method for the synthesis of 3-thioazaspiro[4,5]trienones was developed using Pd nanoparticle catalysts,which are highly efficient,environmentally friendly and recyclable.Alkynes and thiophene phenols are effecti...