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Asymmetric benzylic C(sp3)−H acylation via dual nickel and photoredox catalysis

Asymmetric benzylic C(sp3)−H acylation via dual nickel and photoredox catalysis

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_3c17fee165d643adbb5f5970a04f1828

Asymmetric benzylic C(sp3)−H acylation via dual nickel and photoredox catalysis

About this item

Full title

Asymmetric benzylic C(sp3)−H acylation via dual nickel and photoredox catalysis

Publisher

London: Nature Publishing Group UK

Journal title

Nature communications, 2021-06, Vol.12 (1), p.3536-3536, Article 3536

Language

English

Formats

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

Asymmetric C(sp
3
)−H functionalization is a persistent challenge in organic synthesis. Here, we report an asymmetric benzylic C−H acylation of alkylarenes employing carboxylic acids as acyl surrogates for the synthesis of α-aryl ketones via nickel and photoredox dual catalysis. This mild yet straightforward protocol transforms a diverse arra...

Alternative Titles

Full title

Asymmetric benzylic C(sp3)−H acylation via dual nickel and photoredox catalysis

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_3c17fee165d643adbb5f5970a04f1828

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_3c17fee165d643adbb5f5970a04f1828

Other Identifiers

ISSN

2041-1723

E-ISSN

2041-1723

DOI

10.1038/s41467-021-23887-2

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