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The formation of all-cis-(multi)fluorinated piperidines by a dearomatization–hydrogenation process

The formation of all-cis-(multi)fluorinated piperidines by a dearomatization–hydrogenation process

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6522351

The formation of all-cis-(multi)fluorinated piperidines by a dearomatization–hydrogenation process

About this item

Full title

The formation of all-cis-(multi)fluorinated piperidines by a dearomatization–hydrogenation process

Publisher

London: Nature Publishing Group UK

Journal title

Nature chemistry, 2019-03, Vol.11 (3), p.264-270

Language

English

Formats

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

Piperidines and fluorine substituents are both independently indispensable components in pharmaceuticals, agrochemicals and materials. Logically, the incorporation of fluorine atoms into piperidine scaffolds is therefore an area of tremendous potential. However, synthetic approaches towards the formation of these architectures are often impractical...

Alternative Titles

Full title

The formation of all-cis-(multi)fluorinated piperidines by a dearomatization–hydrogenation process

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6522351

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6522351

Other Identifiers

ISSN

1755-4330

E-ISSN

1755-4349

DOI

10.1038/s41557-018-0197-2

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