2023
DOI: 10.1039/d3cc01050c
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Functionalization of arylacetic acids via directing-group-assisted remote meta-C–H activation

Abstract: Herein, we report the first microwave-assisted remote-CH functionalization aided by a simple nitrile directing template. Notably, the present protocol showed broad substrate scope via enabling the meta-CH arylation, acetoxylation, and...

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Cited by 3 publications
(4 citation statements)
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References 35 publications
(38 reference statements)
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“…7–32 Our group is also active in investigating the C–H functionalization at meta -positions of an aromatic molecule with the help of different nitrile-containing templates. 33–37…”
Section: Introductionmentioning
confidence: 99%
“…7–32 Our group is also active in investigating the C–H functionalization at meta -positions of an aromatic molecule with the help of different nitrile-containing templates. 33–37…”
Section: Introductionmentioning
confidence: 99%
“…In this regard, a seminal study of the application of an end-on nitrile directing group for meta -selective C–H functionalization was reported by Yu et al in 2012 . As a result, numerous research teams have investigated a range of approaches using diverse “directing groups”. Our lab has also been actively working on creating distal- m -C–H activation techniques recently, employing distinct directing groups; this could allow the m -C–H functionalization of aromatic scaffolds through the use of essentially straightforward and detachable aliphatic/aromatic nitrile templates. These findings encouraged us to believe that the biphenyl scaffolds would enable remote meta -selective C–H olefination.…”
Section: Introductionmentioning
confidence: 99%
“…32–34 Recently, our group also invented versatile nitrile directing groups (aliphatic and aromatic), which are reversible/reusable upon C–H activation, followed by subsequent functionalization. 35–38…”
mentioning
confidence: 99%
“…[32][33][34] Recently, our group also invented versatile nitrile directing groups (aliphatic and aromatic), which are reversible/reusable upon C-H activation, followed by subsequent functionalization. [35][36][37][38] On the other hand, sulfonic acids are privileged precursors in chemical biology and molecular pharmacology for synthesizing biological probes and protein inhibitors. 39,40 In addition, being a strong acid, sulfonic acid is widely used as a catalyst in many transformations.…”
mentioning
confidence: 99%