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Palladium-catalyzed native alpha-amino acid derivative-directed arylation/oxidation of benzylic C-H bonds: synthesis of 5-aryl-1,4-benzodiazepin-2-ones  ( SCI-EXPANDED收录 EI收录)   被引量:3

文献类型:期刊文献

英文题名:Palladium-catalyzed native alpha-amino acid derivative-directed arylation/oxidation of benzylic C-H bonds: synthesis of 5-aryl-1,4-benzodiazepin-2-ones

作者:Jiang, Fengxuan[1,2];Xu, Menghua[3];Bei, Wenfeng[1];Cheng, Kai[1];Huang, Lehao[2]

机构:[1]Shaoxing Univ, Inst Appl Chem, Key Lab Alternat Technol Fine Chem Proc, Shaoxing 312000, Zhejiang, Peoples R China;[2]Wenzhou Med Univ, Sch Pharmaceut Sci, Wenzhou 325035, Zhejiang, Peoples R China;[3]China Pharmaceut Univ, Dept Med Chem, State Key Lab Nat Med, Jiangsu Key Lab Bioact Nat Prod Res, Nanjing 210009, Peoples R China

年份:2022

卷号:58

期号:69

起止页码:9638

外文期刊名:CHEMICAL COMMUNICATIONS

收录:SCI-EXPANDED(收录号:WOS:000837412900001)、、EI(收录号:20223412616528)、Scopus(收录号:2-s2.0-85136213915)、WOS、CCR-EXPANDED(收录号:WOS:000837412900001)

基金:We are grateful to the Zhejiang Provincial Natural Science Foundation of China (Grant No. LY18B020010) and the Foundation of Wenzhou Medical University Renji College (Grant RJRC14001) for financial support.

语种:英文

外文摘要:A Pd-catalyzed, native alpha-amino acid derivative-directed benzylic C-H bond arylation/oxidation with aryl iodides was developed. The natural amino acid auxiliary could serve as a desired building block for formation of 5-aryl-1,4-benzodiazepin-2-ones after removal of the trifluoroacetyl protecting group. The bifunctional reaction probably proceeded through a sequential benzylic arylation/oxidation process.

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