Arylglycine-derivative synthesis via oxidative sp(3) C–H functionalization of α-amino esters

An efficient method for the synthesis of arylglycine derivatives is described. The oxidative coupling reactions of naphthols and phenols with α-amino esters proceeded smoothly in the presence of meta-chloroperoxybenzoic acid as an oxidant under ambient conditions, to produce arylglycine derivatives...

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Detalles Bibliográficos
Autores principales: Xu, Zhanwei, Yu, Xiaoqiang, Feng, Xiujuan, Bao, Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2012
Materias:
Letter
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3510987/
https://www.ncbi.nlm.nih.gov/pubmed/23209487
http://dx.doi.org/10.3762/bjoc.8.178
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author Xu, Zhanwei
Yu, Xiaoqiang
Feng, Xiujuan
Bao, Ming
author_facet Xu, Zhanwei
Yu, Xiaoqiang
Feng, Xiujuan
Bao, Ming
author_sort Xu, Zhanwei
collection PubMed
description An efficient method for the synthesis of arylglycine derivatives is described. The oxidative coupling reactions of naphthols and phenols with α-amino esters proceeded smoothly in the presence of meta-chloroperoxybenzoic acid as an oxidant under ambient conditions, to produce arylglycine derivatives in satisfactory yields.
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spelling pubmed-35109872012-12-03 Arylglycine-derivative synthesis via oxidative sp(3) C–H functionalization of α-amino esters Xu, Zhanwei Yu, Xiaoqiang Feng, Xiujuan Bao, Ming Beilstein J Org Chem Letter An efficient method for the synthesis of arylglycine derivatives is described. The oxidative coupling reactions of naphthols and phenols with α-amino esters proceeded smoothly in the presence of meta-chloroperoxybenzoic acid as an oxidant under ambient conditions, to produce arylglycine derivatives in satisfactory yields. Beilstein-Institut 2012-09-18 /pmc/articles/PMC3510987/ /pubmed/23209487 http://dx.doi.org/10.3762/bjoc.8.178 Text en Copyright © 2012, Xu et al. https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Letter
Xu, Zhanwei
Yu, Xiaoqiang
Feng, Xiujuan
Bao, Ming
Arylglycine-derivative synthesis via oxidative sp(3) C–H functionalization of α-amino esters
title Arylglycine-derivative synthesis via oxidative sp(3) C–H functionalization of α-amino esters
title_full Arylglycine-derivative synthesis via oxidative sp(3) C–H functionalization of α-amino esters
title_fullStr Arylglycine-derivative synthesis via oxidative sp(3) C–H functionalization of α-amino esters
title_full_unstemmed Arylglycine-derivative synthesis via oxidative sp(3) C–H functionalization of α-amino esters
title_short Arylglycine-derivative synthesis via oxidative sp(3) C–H functionalization of α-amino esters
title_sort arylglycine-derivative synthesis via oxidative sp(3) c–h functionalization of α-amino esters
topic Letter
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3510987/
https://www.ncbi.nlm.nih.gov/pubmed/23209487
http://dx.doi.org/10.3762/bjoc.8.178
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AT yuxiaoqiang arylglycinederivativesynthesisviaoxidativesp3chfunctionalizationofaaminoesters
AT fengxiujuan arylglycinederivativesynthesisviaoxidativesp3chfunctionalizationofaaminoesters
AT baoming arylglycinederivativesynthesisviaoxidativesp3chfunctionalizationofaaminoesters

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