Literature DB >> 24623387

Palladium(II)-catalyzed ortho-C-H arylation/alkylation of N-benzoyl α-amino ester derivatives.

Luis C Misal Castro1, Naoto Chatani.   

Abstract

The palladium-catalyzed arylation/alkylation of ortho-C-H bonds in N-benzoyl α-amino ester derivatives is described. In such a system both the NH-amido and the CO2R groups in the α-amino ester moieties play a role in successful C-H activation/C-C bond formation using iodoaryl coupling partners. A wide variety of functional groups and electron-rich/deficient iodoarenes are tolerated. The yields obtained range from 20 to 95%.
© 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  CH activation; alkylation; arylation; palladium catalysis; α-amino esters

Mesh:

Substances:

Year:  2014        PMID: 24623387     DOI: 10.1002/chem.201304978

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  4 in total

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2.  Asymmetric C-H functionalization of cyclopropanes using an isoleucine-NH2 bidentate directing group.

Authors:  Jinhee Kim; Mikyung Sim; Namhoon Kim; Sungwoo Hong
Journal:  Chem Sci       Date:  2015-04-16       Impact factor: 9.825

3.  Pd-catalysed ligand-enabled carboxylate-directed highly regioselective arylation of aliphatic acids.

Authors:  Yan Zhu; Xiaolan Chen; Chunchen Yuan; Guobao Li; Jingyu Zhang; Yingsheng Zhao
Journal:  Nat Commun       Date:  2017-04-06       Impact factor: 14.919

4.  Ni(ii)-catalyzed mono-selective ortho-arylation of unactivated aryl C-H bonds utilizing amino acids as a directing group.

Authors:  Zhanqing Cong; Feng Gao; Hong Liu
Journal:  RSC Adv       Date:  2019-04-08       Impact factor: 4.036

  4 in total

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