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Enantioselective amine α-functionalization via palladium-catalysed C–H arylation of thioamides

Enantioselective amine α-functionalization via palladium-catalysed C–H arylation of thioamides

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5347480

Enantioselective amine α-functionalization via palladium-catalysed C–H arylation of thioamides

About this item

Full title

Enantioselective amine α-functionalization via palladium-catalysed C–H arylation of thioamides

Publisher

London: Nature Publishing Group UK

Journal title

Nature chemistry, 2017-02, Vol.9 (2), p.140-144

Language

English

Formats

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

Saturated aza-heterocycles are highly privileged building blocks that are commonly encountered in bioactive compounds and approved therapeutic agents. These N-heterocycles are also incorporated as chiral auxiliaries and ligands in asymmetric synthesis. As such, the development of methods to functionalize the α-methylene C–H bonds of these systems e...

Alternative Titles

Full title

Enantioselective amine α-functionalization via palladium-catalysed C–H arylation of thioamides

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5347480

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5347480

Other Identifiers

ISSN

1755-4330

E-ISSN

1755-4349

DOI

10.1038/nchem.2619

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