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Iodonium Salts: Preparation, Chemoselectivity and Metal-Catalyzed Applications
Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi.ORCID-id: 0000-0002-9999-5137
2014 (Engelska)Doktorsavhandling, sammanläggning (Övrigt vetenskapligt)
Abstract [en]

This thesis concerns the preparation and use of diaryliodonium salts. In Project I various unsymmetrical diaryliodonium salts were reacted with three different nucleophiles in order to study the chemoselectivity of the reactions of the salts. The main focus of this project was to gain a deeper understanding of the underlying factors that affect the chemoselectivity in transition metal-free arylation reactions. They were found to be very nucleophile-dependent. Some nucleophiles were very sensitive to electronic effects, whereas others were sensitive to steric factors. Ultimately, some arenes are never transferred. A very interesting scrambling reaction was also observed under the reaction conditions, where unsymmetrical diaryliodonium salts form symmetrical salts in situ.

Project II details the preparation of N-heteroaryliodonium salts via a one-pot procedure. The salts were designed so that the N-heteroaryl moiety was selectively transferred in applications both with and without transition metals. The chemoselectivity was demonstrated by selective transfer of the pyridyl group onto two different nucleophiles.

The third project in the thesis discusses the synthesis of alkynyl(aryl)iodonium salts and alkynylbenziodoxolones from arylsilanes. This protocol could potentially be a very useful complement to the existing procedures, in which boronic acids are used.

The last part of the thesis (Project IV) describes a C-2 selective arylation of indoles where diaryliodonium salts were used in combination with hetero-geneous palladium catalysis. This transformation was performed in water at ambient temperature to 50 °C, and tolerated variations of both the indole and the diaryliodonium salt. Importantly, several N-H indoles could be arylated. The MCF-supported Pd-catalyst showed very little leaching and it was demonstrated that the main part of the reaction occurred via heterogeneous catalysis.

Ort, förlag, år, upplaga, sidor
Stockholm: Department of Organic Chemistry, Stockholm University , 2014. , s. 75
Nyckelord [en]
Diaryliodonium salts, chemoselectivity, heterogeneous catalysis
Nationell ämneskategori
Organisk kemi
Forskningsämne
organisk kemi
Identifikatorer
URN: urn:nbn:se:su:diva-107694ISBN: 978-91-7447-999-7 (tryckt)OAI: oai:DiVA.org:su-107694DiVA, id: diva2:749581
Disputation
2014-10-24, Magnélisalen, Kemiska övningslaboratoriet, Svante Arrhenius väg 16 B, Stockholm, 10:00 (Engelska)
Opponent
Handledare
Anmärkning

At the time of the doctoral defense, the following papers were unpublished and had a status as follows: Paper 3: Manuscript. Paper 4: Accepted.

Tillgänglig från: 2014-10-02 Skapad: 2014-09-24 Senast uppdaterad: 2014-11-18Bibliografiskt granskad
Delarbeten
1. Arylation with Unsymmetrical Diaryliodonium Salts: A Chemoselectivity Study
Öppna denna publikation i ny flik eller fönster >>Arylation with Unsymmetrical Diaryliodonium Salts: A Chemoselectivity Study
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2013 (Engelska)Ingår i: Chemistry - A European Journal, ISSN 0947-6539, E-ISSN 1521-3765, Vol. 19, nr 31, s. 10334-10342Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Phenols, anilines, and malonates have been arylated under metal-free conditions with twelve aryl(phenyl)iodonium salts in a systematic chemoselectivity study. A new “anti-ortho effect” has been identified in the arylation of malonates. Several “dummy groups” have been found that give complete chemoselectivity in the transfer of the phenyl moiety, irrespective of the nucleophile. An aryl exchange in the diaryliodonium salts has been observed under certain arylation conditions. DFT calculations have been performed to investigate the reaction mechanism and to elucidate the origins of the observed selectivities. These results are expected to facilitate the design of chiral diaryliodonium salts and the development of catalytic arylation reactions that are based on these sustainable and metal-free reagents.

Nyckelord
arylation, chemoselectivity, DFT calculations, hypervalent compounds, ligand exchange
Nationell ämneskategori
Organisk kemi
Forskningsämne
organisk kemi
Identifikatorer
urn:nbn:se:su:diva-75778 (URN)10.1002/chem.201300860 (DOI)000321983700034 ()
Forskningsfinansiär
Vetenskapsrådet, 621-2011-3608
Tillgänglig från: 2012-04-26 Skapad: 2012-04-26 Senast uppdaterad: 2017-12-07Bibliografiskt granskad
2. One-Pot Synthesis and Applications of N-Heteroaryl Iodonium Salts
Öppna denna publikation i ny flik eller fönster >>One-Pot Synthesis and Applications of N-Heteroaryl Iodonium Salts
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2014 (Engelska)Ingår i: ChemistryOpen, ISSN 2191-1363, Vol. 3, nr 1, s. 19-22Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

An efficient one-pot synthesis of N-heteroaryl iodonium triflates from the corresponding N-heteroaryl iodide and arene has been developed. The reaction conditions resemble our previous one-pot syntheses, with suitable modifications to allow N-heteroaryl groups. The reaction time is only 30min, and no anion exchange is required. The obtained iodonium salts were isolated in a protonated form, these salts can either be employed directly in applications or be deprotonated prior to use. The aryl groups were chosen to induce chemoselective transfer of the heteroaryl moiety to various nucleophiles. The reactivity and chemoselectivity of these iodonium salts were demonstrated by selectively introducing a pyridyl moiety onto both oxygen and carbon nucleophiles in good yields.

Nyckelord
arylation, heterocycles, hypervalent iodine, iodonium salts, oxidation
Nationell ämneskategori
Kemi
Forskningsämne
organisk kemi
Identifikatorer
urn:nbn:se:su:diva-105258 (URN)10.1002/open.201300042 (DOI)000333393700003 ()
Forskningsfinansiär
Vetenskapsrådet, 621-2011-3608
Anmärkning

AuthorCount:5;

Tillgänglig från: 2014-06-25 Skapad: 2014-06-24 Senast uppdaterad: 2017-12-05Bibliografiskt granskad
3. Synthesis of Alkynyl(aryl)iodonium salts from TMS-alkynes
Öppna denna publikation i ny flik eller fönster >>Synthesis of Alkynyl(aryl)iodonium salts from TMS-alkynes
(Engelska)Manuskript (preprint) (Övrigt vetenskapligt)
Nationell ämneskategori
Organisk kemi
Forskningsämne
organisk kemi
Identifikatorer
urn:nbn:se:su:diva-107699 (URN)
Tillgänglig från: 2014-09-24 Skapad: 2014-09-24 Senast uppdaterad: 2014-09-25
4. C-2 Selective Arylation of Indoles with Heterogeneous Nanopalladium and Diaryliodonium Salts
Öppna denna publikation i ny flik eller fönster >>C-2 Selective Arylation of Indoles with Heterogeneous Nanopalladium and Diaryliodonium Salts
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2014 (Engelska)Ingår i: Chemistry - A European Journal, ISSN 0947-6539, E-ISSN 1521-3765, Vol. 20, nr 42, s. 13531-13535Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

A simple and efficient method to prepare synthetically useful 2-arylindoles is presented, using a heterogeneous Pd catalyst and diaryliodonium salts in water under mild conditions. A remarkably low leaching of metal catalyst was observed under the applied conditions. The developed protocol is highly C-2 selective and tolerates structural variations both in the indole and in the diaryliodonium salt. Arylations of both NH indoles and N-protected indoles with ortho-substituted, electron-rich, electron-deficient, or halogenated diaryliodonium salts were achieved to give the desired products in high to excellent isolated yields within 6 to 15 h at room temperature or 40 °C.

Ort, förlag, år, upplaga, sidor
Weinheim: , 2014
Nyckelord
arylation, hypervalent iodine, indoles, nanopalladium, palladium catalysis
Nationell ämneskategori
Organisk kemi
Forskningsämne
organisk kemi
Identifikatorer
urn:nbn:se:su:diva-107700 (URN)10.1002/chem.201404017 (DOI)000342797500013 ()
Forskningsfinansiär
Berzelii Centre EXSELENTEU, Europeiska forskningsrådet, ERC AdG 247014Vetenskapsrådet, 621- 2011-3608Vetenskapsrådet, 621-2013-4653
Tillgänglig från: 2014-09-24 Skapad: 2014-09-24 Senast uppdaterad: 2017-12-05Bibliografiskt granskad

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