Direct Dehydrogenative Access to Unsymmetrical Phenones.

Arylation Cross Dehydrogenative Coupling C−H Functionalization Electrochemistry Hexafluoroisopropanol

Journal

Angewandte Chemie (International ed. in English)
ISSN: 1521-3773
Titre abrégé: Angew Chem Int Ed Engl
Pays: Germany
ID NLM: 0370543

Informations de publication

Date de publication:
09 05 2022
Historique:
received: 24 01 2022
pubmed: 8 2 2022
medline: 4 5 2022
entrez: 7 2 2022
Statut: ppublish

Résumé

The first non-directed dehydrogenative phenone coupling method of methylarenes with aromatic C-H bonds, displaying a large substrate scope, is herein reported. This reaction represents a far more direct atom- and step-efficient alternative to the classical Friedel-Crafts or Suzuki-Miyaura derived acylation reactions. The method can be carried out on a gram scale and was successfully applied to the synthesis of several Ketoprofen drug analogues.

Identifiants

pubmed: 35128810
doi: 10.1002/anie.202201142
pmc: PMC9314079
doi:

Substances chimiques

Ketones 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e202201142

Informations de copyright

© 2022 The Authors. Angewandte Chemie International Edition published by Wiley-VCH GmbH.

Références

Chem Commun (Camb). 2015 Feb 4;51(10):1870-3
pubmed: 25526034
Angew Chem Int Ed Engl. 2012 May 21;51(21):5204-7
pubmed: 22488920
Chem Rev. 2018 Jul 25;118(14):6706-6765
pubmed: 29963856
J Am Chem Soc. 2019 May 1;141(17):6869-6874
pubmed: 30983348
Org Lett. 2003 Apr 3;5(7):1103-6
pubmed: 12659584
J Am Chem Soc. 2018 Mar 14;140(10):3724-3735
pubmed: 29461813
Angew Chem Int Ed Engl. 2022 May 9;61(20):e202201142
pubmed: 35128810
Pharmacotherapy. 1986 May-Jun;6(3):93-103
pubmed: 3526298
J Clin Pharmacol. 2004 Jan;44(1):7-19
pubmed: 14681337
Chem Sci. 2017 Sep 1;8(9):6525-6530
pubmed: 28989678
J Org Chem. 2012 Dec 21;77(24):11339-44
pubmed: 23176710
Org Lett. 2010 Aug 20;12(16):3645-7
pubmed: 20669896
J Org Chem. 2017 Apr 7;82(7):3767-3780
pubmed: 28299930
Org Lett. 2017 Mar 17;19(6):1434-1437
pubmed: 28263605
Angew Chem Int Ed Engl. 2018 May 14;57(20):5594-5619
pubmed: 29292849
Org Lett. 2015 Dec 4;17(23):5890-3
pubmed: 26587583
Angew Chem Int Ed Engl. 2014 Jan 3;53(1):74-100
pubmed: 24214829
Chem Rev. 2017 Nov 8;117(21):13230-13319
pubmed: 28991454
J Am Chem Soc. 2017 Jan 25;139(3):1311-1318
pubmed: 28001393
J Org Chem. 2021 Jan 15;86(2):1396-1407
pubmed: 33382269
Chemistry. 2021 Feb 19;27(11):3682-3687
pubmed: 33283370
Chem Commun (Camb). 2014 Dec 18;50(97):15352-4
pubmed: 25348462
J Org Chem. 2015 Aug 7;80(15):7810-5
pubmed: 26166246
Org Lett. 2003 Nov 27;5(24):4645-8
pubmed: 14627405
Chem Soc Rev. 2011 Oct;40(10):4986-5009
pubmed: 21792459
Org Lett. 2012 Oct 19;14(20):5294-7
pubmed: 23020217
Nat Chem. 2018 Feb;10(2):193-199
pubmed: 29359763
Angew Chem Int Ed Engl. 2015 Oct 19;54(43):12664-8
pubmed: 26333071
Angew Chem Int Ed Engl. 2010 Sep 24;49(40):7316-9
pubmed: 20740517
Chemistry. 2016 Jul 18;22(30):10420-4
pubmed: 27304392
Angew Chem Int Ed Engl. 2013 Sep 16;52(38):9900-30
pubmed: 23852649
Chem Commun (Camb). 2014 Apr 14;50(29):3874-7
pubmed: 24589544
Angew Chem Int Ed Engl. 2009;48(23):4114-33
pubmed: 19431166
Food Chem Toxicol. 2003 May;41(5):611-9
pubmed: 12659713
Nat Commun. 2020 Jun 1;11(1):2706
pubmed: 32483217
J Org Chem. 2002 Aug 9;67(16):5616-20
pubmed: 12153259
Angew Chem Int Ed Engl. 2013 Jun 17;52(25):6413-6
pubmed: 23649825
ChemCatChem. 2018 Apr 9;10(7):1547-1551
pubmed: 29731952
Angew Chem Int Ed Engl. 2012 Jul 16;51(29):7259-62
pubmed: 22689181
Angew Chem Int Ed Engl. 2013 Jun 10;52(24):6293-7
pubmed: 23629872
Chem Rev. 2013 Oct 9;113(10):7421-69
pubmed: 23767849
Chem Sci. 2020 May 20;11(46):12386-12400
pubmed: 34123227
Chem Rev. 2011 Mar 9;111(3):1215-92
pubmed: 21391561
Chem Soc Rev. 2020 Mar 21;49(6):1643-1652
pubmed: 32115586
ACS Catal. 2018 Feb 2;8(2):1003-1008
pubmed: 29682398
Chem Soc Rev. 2015 Nov 21;44(22):8062-96
pubmed: 26377280
ACS Catal. 2016 May 6;6(5):3176-3179
pubmed: 32257581
Recent Pat Inflamm Allergy Drug Discov. 2010 Jan;4(1):58-64
pubmed: 19832694
J Org Chem. 2014 Apr 4;79(7):2955-62
pubmed: 24601603
Acc Chem Res. 2019 Oct 15;52(10):2858-2869
pubmed: 31573791
Chem Commun (Camb). 2011 Oct 7;47(37):10461-3
pubmed: 21850348
Org Lett. 2017 May 5;19(9):2426-2429
pubmed: 28445061
Chem Rec. 2020 Feb;20(2):142-161
pubmed: 31264354
J Org Chem. 2013 Oct 18;78(20):10310-8
pubmed: 24004340
Chem Commun (Camb). 2013 Jan 25;49(7):689-91
pubmed: 23230572
Acc Chem Res. 2018 Oct 16;51(10):2589-2599
pubmed: 30240190
Drug Saf. 2012 Sep 1;35(9):759-67
pubmed: 22830618
Org Lett. 2013 Nov 1;15(21):5444-7
pubmed: 24117421
Acc Chem Res. 2020 Jan 21;53(1):72-83
pubmed: 31823612
J Nat Prod. 2015 Jun 26;78(6):1370-82
pubmed: 26039921

Auteurs

Congjun Yu (C)

Institute of Organic Chemistry, RWTH Aachen University, Landoltweg 1, 52074, Aachen, Germany.

Raolin Huang (R)

Institute of Organic Chemistry, RWTH Aachen University, Landoltweg 1, 52074, Aachen, Germany.

Frederic W Patureau (FW)

Institute of Organic Chemistry, RWTH Aachen University, Landoltweg 1, 52074, Aachen, Germany.

Articles similaires

Printing, Three-Dimensional Ketones Benzophenones Polymers Polyethylene Glycols
Dogs Animals Benzophenones Ketones Mandibular Osteotomy
Finite Element Analysis Range of Motion, Articular Humans Lumbar Vertebrae Zygapophyseal Joint

Classifications MeSH