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Concerted nucleophilic aromatic substitutions

Concerted nucleophilic aromatic substitutions

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6105541

Concerted nucleophilic aromatic substitutions

About this item

Full title

Concerted nucleophilic aromatic substitutions

Publisher

London: Nature Publishing Group UK

Journal title

Nature chemistry, 2018-09, Vol.10 (9), p.917-923

Language

English

Formats

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

Nucleophilic aromatic substitution (S
N
Ar) is one of the most widely applied reaction classes in pharmaceutical and chemical research, providing a broadly useful platform for the modification of aromatic ring scaffolds. The generally accepted mechanism for S
N
Ar reactions involves a two-step addition–elimination sequence via a discret...

Alternative Titles

Full title

Concerted nucleophilic aromatic substitutions

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6105541

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6105541

Other Identifiers

ISSN

1755-4330

E-ISSN

1755-4349

DOI

10.1038/s41557-018-0079-7

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