Synthesis of


Journal

Organic letters
ISSN: 1523-7052
Titre abrégé: Org Lett
Pays: United States
ID NLM: 100890393

Informations de publication

Date de publication:
16 Jun 2021
Historique:
entrez: 16 6 2021
pubmed: 17 6 2021
medline: 17 6 2021
Statut: aheadofprint

Résumé

The cubane ring has received intense attention as a 3D benzene isostere and scaffold. Mono- and 1,4-disubstituted cubanes are well-described. Here we report a practical procedure for a direct radical-mediated chlorocarbonylation process initially reported by Bashir-Hashemi, to access a range of 2-substituted 1,4-cubanedicarboxylic ester derivatives. A subsequent regioselective ester hydrolysis to give fully differentiated 1,2,4-trisubstituted cubanes is demonstrated.

Identifiants

pubmed: 34133174
doi: 10.1021/acs.orglett.1c01702
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Diego E Collin (DE)

School of Chemistry, University of Southampton, Highfield, Southampton SO17 1BJ, United Kingdom.

Kristina Kovacic (K)

School of Chemistry, University of Southampton, Highfield, Southampton SO17 1BJ, United Kingdom.

Mark E Light (ME)

School of Chemistry, University of Southampton, Highfield, Southampton SO17 1BJ, United Kingdom.

Bruno Linclau (B)

School of Chemistry, University of Southampton, Highfield, Southampton SO17 1BJ, United Kingdom.

Classifications MeSH