Synthesis of β-arylated alkylamides via Pd-catalyzed one-pot installation of a directing group and C(sp3)–H arylation

The synthesis of β-arylated alkylamides via alkyl C–H bond arylation has been realized by means of direct one-pot reactions of acyl chlorides, aryl iodides and 8-aminoquinoline. Depending on the structure of the starting materials, both single and double β-arylated alkylamides could be accessed.

Bibliographic Details
Main Authors: Yunyun Liu, Yi Zhang, Xiaoji Cao, Jie-Ping Wan
Format: Article
Language:English
Published: Beilstein-Institut 2016-06-01
Series:Beilstein Journal of Organic Chemistry
Subjects:
Online Access:https://doi.org/10.3762/bjoc.12.108
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spelling doaj-35479b0d539d49ac8645c2285f7b4d892021-02-02T08:28:38ZengBeilstein-InstitutBeilstein Journal of Organic Chemistry1860-53972016-06-011211122112610.3762/bjoc.12.1081860-5397-12-108Synthesis of β-arylated alkylamides via Pd-catalyzed one-pot installation of a directing group and C(sp3)–H arylationYunyun Liu0Yi Zhang1Xiaoji Cao2Jie-Ping Wan3College of Chemistry and Chemical Engineering, Jiangxi Normal University, Nanchang 330022 P. R. ChinaCollege of Chemistry and Chemical Engineering, Jiangxi Normal University, Nanchang 330022 P. R. ChinaResearch Center of Analysis and Measurement, Zhejiang University of Technology, 18 Chaowang Road, Hangzhou, Zhejiang 310014, P.R. ChinaCollege of Chemistry and Chemical Engineering, Jiangxi Normal University, Nanchang 330022 P. R. ChinaThe synthesis of β-arylated alkylamides via alkyl C–H bond arylation has been realized by means of direct one-pot reactions of acyl chlorides, aryl iodides and 8-aminoquinoline. Depending on the structure of the starting materials, both single and double β-arylated alkylamides could be accessed.https://doi.org/10.3762/bjoc.12.108alkylamidesC–H arylationdirecting groupin situ installationone-pot
collection DOAJ
language English
format Article
sources DOAJ
author Yunyun Liu
Yi Zhang
Xiaoji Cao
Jie-Ping Wan
spellingShingle Yunyun Liu
Yi Zhang
Xiaoji Cao
Jie-Ping Wan
Synthesis of β-arylated alkylamides via Pd-catalyzed one-pot installation of a directing group and C(sp3)–H arylation
Beilstein Journal of Organic Chemistry
alkylamides
C–H arylation
directing group
in situ installation
one-pot
author_facet Yunyun Liu
Yi Zhang
Xiaoji Cao
Jie-Ping Wan
author_sort Yunyun Liu
title Synthesis of β-arylated alkylamides via Pd-catalyzed one-pot installation of a directing group and C(sp3)–H arylation
title_short Synthesis of β-arylated alkylamides via Pd-catalyzed one-pot installation of a directing group and C(sp3)–H arylation
title_full Synthesis of β-arylated alkylamides via Pd-catalyzed one-pot installation of a directing group and C(sp3)–H arylation
title_fullStr Synthesis of β-arylated alkylamides via Pd-catalyzed one-pot installation of a directing group and C(sp3)–H arylation
title_full_unstemmed Synthesis of β-arylated alkylamides via Pd-catalyzed one-pot installation of a directing group and C(sp3)–H arylation
title_sort synthesis of β-arylated alkylamides via pd-catalyzed one-pot installation of a directing group and c(sp3)–h arylation
publisher Beilstein-Institut
series Beilstein Journal of Organic Chemistry
issn 1860-5397
publishDate 2016-06-01
description The synthesis of β-arylated alkylamides via alkyl C–H bond arylation has been realized by means of direct one-pot reactions of acyl chlorides, aryl iodides and 8-aminoquinoline. Depending on the structure of the starting materials, both single and double β-arylated alkylamides could be accessed.
topic alkylamides
C–H arylation
directing group
in situ installation
one-pot
url https://doi.org/10.3762/bjoc.12.108
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