Bobbitt's Salt-Mediated Oxidation of Alkynyl-ols and -diols to the Corresponding Aldehydes and Their Application in Tandem Reactions.


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:
03 Mar 2023
Historique:
pubmed: 23 2 2023
medline: 23 2 2023
entrez: 22 2 2023
Statut: ppublish

Résumé

Propargyl alcohol derivatives were readily oxidized using Bobbitt's salt to yield the corresponding propynal products. 2-Butyn-1,4-diol may be selectively oxidized to provide either 4-hydroxy-2-butynal or acetylene dicarboxaldehyde, and the resulting stable dichloromethane solutions containing the chemically sensitive acetylene aldehydes were used directly in subsequent Wittig, Grignard, or Diels-Alder reactions. This method provides safe and efficient access to propynals and allows the preparation of polyfunctional acetylene compounds from readily accessible starting material without the use of protecting groups.

Identifiants

pubmed: 36812364
doi: 10.1021/acs.joc.2c02828
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

3321-3325

Auteurs

James M Bobbitt (JM)

Department of Chemistry, University of Connecticut, Storrs, Connecticut 06269-3060, United States.

Nicholas A Eddy (NA)

Department of Chemistry, University of Connecticut, Storrs, Connecticut 06269-3060, United States.

Christian Brückner (C)

Department of Chemistry, University of Connecticut, Storrs, Connecticut 06269-3060, United States.

William F Bailey (WF)

Department of Chemistry, University of Connecticut, Storrs, Connecticut 06269-3060, United States.

Nabyl Merbouh (N)

Department of Chemistry, Simon Fraser University, Burnaby, British Columbia V5A 1S6, Canada.

Classifications MeSH