Synthesis of Fluorinated 3,6-Dihydropyridines and 2-(Fluoromethyl)pyridines by Electrophilic Fluorination of 1,2-Dihydropyridines with Selectfluor

Selectfluor® dihydropyridines electrophilic fluorination fluorine-containing heterocycles homoallyl long-range coupling

Journal

Molecules (Basel, Switzerland)
ISSN: 1420-3049
Titre abrégé: Molecules
Pays: Switzerland
ID NLM: 100964009

Informations de publication

Date de publication:
09 Jul 2020
Historique:
received: 04 06 2020
revised: 08 07 2020
accepted: 08 07 2020
entrez: 15 7 2020
pubmed: 15 7 2020
medline: 26 2 2021
Statut: epublish

Résumé

New fluorinated 3,6-dihydropyridines were obtained by the electrophilic fluorination of 1,2-dihydropyridines with Selectfluor

Identifiants

pubmed: 32660085
pii: molecules25143143
doi: 10.3390/molecules25143143
pmc: PMC7397266
pii:
doi:

Substances chimiques

Dihydropyridines 0
Hydrocarbons, Fluorinated 0
Fluorine 284SYP0193

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : State Education Development Agency Republic of Latvia
ID : PostDoc project Nr.1.1.1.2/VIAA/2/18/373

Références

Angew Chem Int Ed Engl. 2001 Dec 3;40(23):4461-4463
pubmed: 12404445
J Am Chem Soc. 2006 May 3;128(17):5851-8
pubmed: 16637654
J Org Chem. 2019 Nov 1;84(21):13516-13527
pubmed: 31556607
J Chem Phys. 2010 Apr 21;132(15):154104
pubmed: 20423165
J Am Chem Soc. 2001 Jul 25;123(29):7001-9
pubmed: 11459478
J Org Chem. 2018 Jun 15;83(12):6762-6768
pubmed: 29768006
J Org Chem. 2012 Oct 19;77(20):9148-55
pubmed: 23030737
Nucleosides Nucleotides Nucleic Acids. 2004;23(1-2):161-70
pubmed: 15043144
Chemistry. 1996 May;2(5):516-522
pubmed: 29178226
Org Lett. 2000 Mar 9;2(5):639-42
pubmed: 10814398
Tetrahedron. 2011 Jun 17;67(24):4449-4454
pubmed: 21691436
Org Lett. 2017 Mar 17;19(6):1410-1413
pubmed: 28256137
Bioorg Med Chem Lett. 2012 Dec 15;22(24):7742-7
pubmed: 23122860

Auteurs

Nadiia V Pikun (NV)

Latvian Institute of Organic Synthesis, Aizkraukles Str. 21, LV-1006 Riga, Latvia.

Arkadij Sobolev (A)

Latvian Institute of Organic Synthesis, Aizkraukles Str. 21, LV-1006 Riga, Latvia.

Aiva Plotniece (A)

Latvian Institute of Organic Synthesis, Aizkraukles Str. 21, LV-1006 Riga, Latvia.

Martins Rucins (M)

Latvian Institute of Organic Synthesis, Aizkraukles Str. 21, LV-1006 Riga, Latvia.

Brigita Vigante (B)

Latvian Institute of Organic Synthesis, Aizkraukles Str. 21, LV-1006 Riga, Latvia.

Marina Petrova (M)

Latvian Institute of Organic Synthesis, Aizkraukles Str. 21, LV-1006 Riga, Latvia.

Ruslan Muhamadejev (R)

Latvian Institute of Organic Synthesis, Aizkraukles Str. 21, LV-1006 Riga, Latvia.

Karlis Pajuste (K)

Latvian Institute of Organic Synthesis, Aizkraukles Str. 21, LV-1006 Riga, Latvia.

Yuriy G Shermolovich (YG)

Institute of Organic Chemistry NAS of Ukraine, Murmanska Str. 5, 02660 Kyiv, Ukraine.

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Classifications MeSH