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Manganese-mediated reductive functionalization of activated aliphatic acids and primary amines

Manganese-mediated reductive functionalization of activated aliphatic acids and primary amines

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_89f05c7d9acb4c02bc6f16d5f62bae88

Manganese-mediated reductive functionalization of activated aliphatic acids and primary amines

About this item

Full title

Manganese-mediated reductive functionalization of activated aliphatic acids and primary amines

Publisher

London: Nature Publishing Group UK

Journal title

Nature communications, 2020-10, Vol.11 (1), p.5036-5036, Article 5036

Language

English

Formats

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

Alkyl carboxylic acids as well as primary amines are ubiquitous in all facets of biological science, pharmaceutical science, chemical science and materials science. By chemical conversion to redox-active esters (RAE) and Katritzky’s
N
-alkylpyridinium salts, respectively, alkyl carboxylic acids and primary amines serve as ideal starting mater...

Alternative Titles

Full title

Manganese-mediated reductive functionalization of activated aliphatic acids and primary amines

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_89f05c7d9acb4c02bc6f16d5f62bae88

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_89f05c7d9acb4c02bc6f16d5f62bae88

Other Identifiers

ISSN

2041-1723

E-ISSN

2041-1723

DOI

10.1038/s41467-020-18834-6

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