Impact of C-H Cross-Coupling Reactions in the One-Step Retrosynthesis of Drug Molecules.


Journal

The Journal of organic chemistry
ISSN: 1520-6904
Titre abrégé: J Org Chem
Pays: United States
ID NLM: 2985193R

Informations de publication

Date de publication:
14 Oct 2024
Historique:
medline: 14 10 2024
pubmed: 14 10 2024
entrez: 14 10 2024
Statut: aheadofprint

Résumé

Pharmaceutical synthesis requires a diversity of chemical reactions. The discovery of new reactions enable novel retrosynthetic disconnections, potentially expediting access to complex molecules. This Synopsis demonstrates the use of enumerative combinatorics to find impactful underdeveloped reactions for drug synthesis. By mapping pharmaceutical target molecules onto available building blocks using just one retrosynthetic disconnection even if the requisite reaction is not yet known, we highlight the importance of site-selective C-H cross-coupling methods. This cheminformatics-driven retrosynthetic analysis identifies novel reaction methods of value to the synthesis toolbox.

Identifiants

pubmed: 39401427
doi: 10.1021/acs.joc.4c01567
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Babak Mahjour (B)

Department of Medicinal Chemistry, University of Michigan, Ann Arbor, Michigan 48109, United States.

Kaitlyn M Flynn (KM)

Department of Chemistry, University of Wisconsin─Madison, Madison, Wisconsin 53706, United States.

Shannon S Stahl (SS)

Department of Chemistry, University of Wisconsin─Madison, Madison, Wisconsin 53706, United States.

Tim Cernak (T)

Department of Medicinal Chemistry, University of Michigan, Ann Arbor, Michigan 48109, United States.

Classifications MeSH