Heavier Carbonyl Olefination: The Sila-Wittig Reaction.


Journal

Journal of the American Chemical Society
ISSN: 1520-5126
Titre abrégé: J Am Chem Soc
Pays: United States
ID NLM: 7503056

Informations de publication

Date de publication:
23 10 2019
Historique:
pubmed: 29 9 2019
medline: 29 9 2019
entrez: 28 9 2019
Statut: ppublish

Résumé

The Wittig reaction is one of the most versatile tools in the repertoire of organic chemists. Thus, a broad variety of carbonyl compounds can be converted to tailor-made alkenes with phosphorus ylides under mild conditions. However, no comparable reaction has been reported for silanones, the silicon congeners of ketones. Here, we demonstrate for the first time the successful application of the Wittig olefination to iminosilylsilanone

Identifiants

pubmed: 31560854
doi: 10.1021/jacs.9b09379
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

16991-16996

Auteurs

Dominik Reiter (D)

Department of Chemistry, WACKER-Institute of Silicon Chemistry and Catalysis Research Center , Technische Universität München , Lichtenbergstraße 4 , 85748 Garching bei München , Germany.

Philipp Frisch (P)

Department of Chemistry, WACKER-Institute of Silicon Chemistry and Catalysis Research Center , Technische Universität München , Lichtenbergstraße 4 , 85748 Garching bei München , Germany.

Tibor Szilvási (T)

Department of Chemical and Biological Engineering , University of Wisconsin-Madison , 1415 Engineering Drive , Madison , Wisconsin 53706-1607 , United States.

Shigeyoshi Inoue (S)

Department of Chemistry, WACKER-Institute of Silicon Chemistry and Catalysis Research Center , Technische Universität München , Lichtenbergstraße 4 , 85748 Garching bei München , Germany.

Classifications MeSH