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
About this item
Full title
Author / Creator
Publisher
London: Nature Publishing Group UK
Journal title
Language
English
Formats
Publication information
Publisher
London: Nature Publishing Group UK
Subjects
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
Authors, Artists and Contributors
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