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Accessing three-dimensional molecular diversity through benzylic C–H cross-coupling

Accessing three-dimensional molecular diversity through benzylic C–H cross-coupling

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2955268939

Accessing three-dimensional molecular diversity through benzylic C–H cross-coupling

About this item

Full title

Accessing three-dimensional molecular diversity through benzylic C–H cross-coupling

Publisher

England: Nature Publishing Group

Journal title

Nature Synthesis, 2023-10, Vol.2 (10), p.998-1008

Language

English

Formats

Publication information

Publisher

England: Nature Publishing Group

More information

Scope and Contents

Contents

Pharmaceutical and agrochemical discovery efforts rely on robust methods for chemical synthesis that rapidly access diverse molecules
. Cross-coupling reactions are the most widely used synthetic methods
, but these methods typically form bonds to C(
)-hybridized carbon atoms (e.g., amide coupling, biaryl coupling) and lead to a prevalence...

Alternative Titles

Full title

Accessing three-dimensional molecular diversity through benzylic C–H cross-coupling

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_miscellaneous_2955268939

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_2955268939

Other Identifiers

ISSN

2731-0582

E-ISSN

2731-0582

DOI

10.1038/s44160-023-00332-4

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