Literature DB >> 26984111

Dehydrogenative Cross-Coupling Reaction between N-Aryl α-Amino Acid Esters and Phenols or Phenol Derivative for Synthesis of α-Aryl α-Amino Acid Esters.

Muhammad Salman1, Zhi-Qiang Zhu1, Zhi-Zhen Huang1,2.   

Abstract

A novel dehydrogenative cross-coupling (DCC) reaction between N-arylglycine esters and phenols or 1,3,5-trimethoxybenzene was developed by copper catalysis using di-tert-butyl peroxide (DTBP) as an oxidant. Under optimized conditions, a range of N-arylglycine esters 1 underwent the DCC reaction smoothly with various phenols 2 or 1,3,5-trimethoxybenzene 4 to give desired α-aryl α -amino acid esters 3 or 5, respectively, with high ortho regioselectivities in a moderate to excellent yield. A possible mechanism involving aromatic electrophilic substitution is proposed.

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Year:  2016        PMID: 26984111     DOI: 10.1021/acs.orglett.6b00162

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  3 in total

1.  Functionalization of N-arylglycine esters: electrocatalytic access to C-C bonds mediated by n-Bu4NI.

Authors:  Mi-Hai Luo; Yang-Ye Jiang; Kun Xu; Yong-Guo Liu; Bao-Guo Sun; Cheng-Chu Zeng
Journal:  Beilstein J Org Chem       Date:  2018-02-22       Impact factor: 2.883

2.  Palladium-catalyzed oxidative cross-coupling for the synthesis of α-amino ketones.

Authors:  Xiao-Hong Wei; Zhen-Hua Li; Lian-Biao Zhao; Ping Zhang; Han-Cheng Zhou; Yan-Bin Wang
Journal:  RSC Adv       Date:  2019-10-09       Impact factor: 4.036

3.  Ketoxime peptide ligations: oxidative couplings of alkoxyamines to N-aryl peptides.

Authors:  Quibria A E Guthrie; Hailey A Young; Caroline Proulx
Journal:  Chem Sci       Date:  2019-08-29       Impact factor: 9.825

  3 in total

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