Mild and Low-Pressure fac-Ir(ppy)3 -Mediated Radical Aminocarbonylation of Unactivated Alkyl Iodides through Visible-Light Photoredox Catalysis. (Q48210732)

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English	Mild and Low-Pressure fac-Ir(ppy)3 -Mediated Radical Aminocarbonylation of Unactivated Alkyl Iodides through Visible-Light Photoredox Catalysis.	scientific article

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scholarly article

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Europe PubMed Central

9 February 2018

http://europepmc.org/abstract/MED/27271773

Mild and Low-Pressure fac-Ir(ppy)3 -Mediated Radical Aminocarbonylation of Unactivated Alkyl Iodides through Visible-Light Photoredox Catalysis. (English)

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Europe PubMed Central

9 February 2018

http://europepmc.org/abstract/MED/27271773

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8 June 2020

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author name string

Linda Åkerbladh

3

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8 June 2020

Sara Bergman

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8 June 2020

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7 June 2016

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Chemistry—A European Journal

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8 June 2020

9155-9161

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8 June 2020

Direct synthesis of amides from carboxylic acids and amines using B(OCH2CF3)3.

1 reference

https://api.crossref.org/works/10.1002%2FCHEM.201601694

21 January 2018

Amide bond formation and peptide coupling

1 reference

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N-heterocyclic carbene-catalyzed redox amidations of alpha-functionalized aldehydes with amines

1 reference

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Nucleophilic carbene and HOAt relay catalysis in an amide bond coupling: an orthogonal peptide bond forming reaction

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The mechanism of the lithium - halogen Interchange reaction : a review of the literature

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Highly functionalized organomagnesium reagents prepared through halogen-metal exchange

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Engaging unactivated alkyl, alkenyl and aryl iodides in visible-light-mediated free radical reactions.

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Discovery and development of telaprevir: an NS3-4A protease inhibitor for treating genotype 1 chronic hepatitis C virus

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Convenient Method for the Preparation of Weinreb Amides via Pd-Catalyzed Aminocarbonylation of Aryl Bromides at Atmospheric Pressure

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Palladium-catalyzed carbonylation reactions of aryl halides and related compounds

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Molybdenum-mediated carbonylation of aryl halides with nucleophiles using microwave irradiation

1 reference

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21 January 2018

Mo(CO)(6)-mediated carbamoylation of aryl halides.

1 reference

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Radical-mediated carboxylation of alkyl iodides with [11C]carbon monoxide in solvent mixtures

1 reference

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Carbonylation reactions of alkyl iodides through the interplay of carbon radicals and Pd catalysts.

1 reference

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Catalysis of Radical Reactions: A Radical Chemistry Perspective

1 reference

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Visible light photoredox catalysis with transition metal complexes: applications in organic synthesis

1 reference

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Selective fluorination of alkyl C-H bonds via photocatalysis.

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The frequently overlooked importance of solvent in free radical syntheses.

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21 January 2018

Can decarbonylation of acyl radicals be overcome in radical addition reactions? En route to a solution employing N-acyl oxazolidinones and SmI2/H2O.

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Synthesis and bioassay of improved mosquito repellents predicted from chemical structure

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Carboxamides combining favorable olfactory properties with insect repellency

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Reductive carbonylation of aryl halides employing a two-chamber reactor: a protocol for the synthesis of aryl aldehydes including 13C- and D-isotope labeling

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21 January 2018

Iron-catalyzed oxidative amidation of tertiary amines with aldehydes

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21 January 2018

A novel Pd-catalyzed N-dealkylative carbonylation of tertiary amines for the preparation of amides.

1 reference

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21 January 2018

The chemistry of amine radical cations produced by visible light photoredox catalysis.

1 reference

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Discovery and biological evaluation of adamantyl amide 11β-HSD1 inhibitors

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Mechanistic investigation of the oxidation of hydrazides: implications for the activation of the TB drug isoniazid

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Identifiers

10.1002/CHEM.201601694

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27271773%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

10.1002/CHEM.201601694

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1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27271773%20AND%20SRC:MED&resulttype=core&format=json

8 June 2020

2-s2.0-84977495975

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