Origins of Diastereoselectivity in the Addition of Enoxysilanes to Vinyl Diazonium Salts.


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:
13 Jul 2024
Historique:
medline: 14 7 2024
pubmed: 14 7 2024
entrez: 13 7 2024
Statut: aheadofprint

Résumé

The addition of enoxysilanes to vinyl diazonium ions occurs with varying levels of diastereoselectivity. To understand the origins of the stereoselectivity, we studied these transformations using density functional theory (DFT) calculations. The selectivity stems from a stabilizing cation-π interaction that orients the nucleophile and the diazonium ion.

Identifiants

pubmed: 39002159
doi: 10.1021/acs.joc.4c00874
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Avery Peck (A)

Department of Chemistry, University of Vermont, 82 University Place, Burlington, Vermont 05495, United States.

Manman Sun (M)

Center of Chemistry for Frontier Technologies, Department of Chemistry, State Key Laboratory of Clean Energy Utilization, Zhejiang University, Hangzhou 310027, China.
Advanced Research Institute and School of Pharmaceutical Science, Taizhou University, Jiaojiang, Zhejiang 318000, China.

Evan Howard (E)

Department of Chemistry, University of Vermont, 82 University Place, Burlington, Vermont 05495, United States.

Xin Hong (X)

Center of Chemistry for Frontier Technologies, Department of Chemistry, State Key Laboratory of Clean Energy Utilization, Zhejiang University, Hangzhou 310027, China.
Beijing National Laboratory for Molecular Sciences, Zhongguancun North First Street No. 2, Beijing 100190, China.
State Key Laboratory of Physical Chemistry of Solid Surfaces, Xiamen University, Xiamen 361005, China.

Matthias Brewer (M)

Department of Chemistry, University of Vermont, 82 University Place, Burlington, Vermont 05495, United States.

Classifications MeSH