support from the National Natural Science Foundation of China(22377113,21927811,22134004);the Taishan Scholar Program of Shandong Province(tsqn202306103);the Fundamental Research Funds for the Central Universities(Ocean University of China)is greatly appreciated.
3,3-Disubstituted oxindoles,forming the core of extensive bioactive natural products and drugs,attract tremendous efforts to develop efficient methods for their preparation.Here,a photocatalyst-free approach for the s...
funded by National Natural Science Foundation of China(No.22201070).
The difunctionalization of bicyclo[1.1.0]butanes is an under-explored transformation that accesses to moieties that are otherwise difficult to prepare.Herein,a new oxidative radical alkylarylation of N-aryl bicyclobut...
National Natural Science Foundation of China(No.22101133);Natural Science Foundation of Jiangsu Province(No.BK20200768)and Nanjing Forestry University are greatly acknowledged.
An efficiently catalytic method toward the synthesis of indolin-2-ones featuring an allylic derived C_(3)-quaternary stereocenter via an intramolecular Heck cyclization/Suzuki coupling of N-substituted-N-(2-bromopheny...
An efficient C-3 sulfuration of oxindoles has been developed.Using disulfide as the sulfurating agent,a wide range of sulfurated oxindoles have been synthesized under t-BuOK/N,N-dimethylformamide(DMF)promoted conditio...
the National Natural Science Foundation of China(Nos.82003592(TS),92056201(WH)and 82201376(SC));Key-Area Research and Development Program of Guangdong Province(No.2022B1111050003)(WH);Shenzhen Science and Technology Innovation Project(No.20200812143116001)(SC);Basic Research Foundation of Guangdong province(No.2021A1515011129)(SC).
We herein reported a sustainable synthesis of 3,3-disubstituted oxindoles via a Michael-type reaction based on the CuBr-catalysed capture of carboxylic oxonium ylides with isatylidene malononitrile.The reaction is cha...
supported by the National Key R&D Program of China (2021YFA1500100);the Strategic Priority Research Program of the Chinese Academy of Sciences (XDB0610000);the National Natural Science Foundation of China (92256303, 22171278, 21821002);the Shanghai Science and Technology Committee (23ZR1482400);the Natural Science Foundation of Ningbo (2023J034)。
By virtue of the atom-and step-economy, utilization of simple arenes as a supplant of pre-prepared aryl metal species or aryl halides for the synthesis of arylated chiral molecules has attracted great attention from t...
the financial supports from the National Natural Science Foundation of China(No.21761132021).
A novel electrochemical multicomponent cascade reaction of indole-tethered alkenes with CF_(3)SO_(2)Na and n-BuaNI has been developed,which enables the rapid assembly of spiropyrrolidinyl-oxindoles in good yields.The ...
supported by the National Natural Science Foundation of China(No.22293011).
Herein,we report an efficient and practical protocol for the photoinduced dehalocyclization of ortho-halophenylacrylamides with formate by the engagement of a CO_(2) radical anion to access substituted oxindoles.This ...
supported by the National Natural Science Foundation of China(21871188,21921002);the Sichuan Science and Technology Program(2021YJ0561);the Sichuan University(2020SCUNL204)。
A highly chemo-and enantioselective alkylation of vinyl azides with 3-bromo-3-substituted oxindoles was achieved through a chiral N,N′-dioxide/Ni(OTf)2-mediated conjugate addition/water addition/elimination tandem pr...
We thank the financial supports from the Natural Science Foundationof Zhejiang Province(LY21B020010).
A general and straightforward strategy for the synthesis of thioester-substituted oxindoles via a palladium-catalyzed thiocarbonyla-tive cyclization process has been developed.With sulfonyl chlorides as promising sulf...