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Silver-Promoted (4+1) Annulation of Isocyanoacetates with Alkylpyridinium Salts: Divergent Regioselective Synthesis of 1,2-Disubstituted Indolizines
Jiangsu Normal Univ, Sch Chem & Mat Sci, Xuzhou 221116, Jiangsu, Peoples R China..
KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Chemistry, Organic chemistry.ORCID iD: 0000-0002-7249-7437
Jiangsu Normal Univ, Sch Chem & Mat Sci, Xuzhou 221116, Jiangsu, Peoples R China..ORCID iD: 0000-0002-5533-2075
KTH, School of Engineering Sciences in Chemistry, Biotechnology and Health (CBH), Chemistry, Organic chemistry.ORCID iD: 0000-0002-6089-5454
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2021 (English)In: Organic Letters, ISSN 1523-7060, E-ISSN 1523-7052, Vol. 23, no 19, p. 7555-7560Article in journal (Refereed) Published
Abstract [en]

An unprecedented silver-promoted regioselective (4 + 1) annulation of isocyanoacetates with pyridinium salts is reported. The established protocol provides controlled, facile, and modular access to a range of synthetically useful N-fused heterocyclic scaffolds containing indolizines, pyrrolo[1,2-a]quinolines, pyrrolo[2,1-a]isoquinolines, and 1H-imidazo[4,5-a]indolizin-2(3H)-ones. A mechanistic pathway involving nucleophilic addition/protonation/elimination/cydoisomerization is proposed.

Place, publisher, year, edition, pages
American Chemical Society (ACS) , 2021. Vol. 23, no 19, p. 7555-7560
National Category
Organic Chemistry
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URN: urn:nbn:se:kth:diva-304195DOI: 10.1021/acs.orglett.1c02754ISI: 000704710800046PubMedID: 34524832Scopus ID: 2-s2.0-85116025460OAI: oai:DiVA.org:kth-304195DiVA, id: diva2:1608201
Note

QC 20211103

Available from: 2021-11-03 Created: 2021-11-03 Last updated: 2023-05-03Bibliographically approved

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Shatskiy, AndreyLiu, JianquanKärkäs, Markus D.

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