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Arbuzov meets 1,2-oxaphosphetanes: transient 1,2-oxaphosphetan-2-iums as an entry point to beta-halo phosphane oxides and P-containing oligomers.
Gleim, Florian; Schnakenburg, Gregor; Ferao, Arturo Espinosa; Streubel, Rainer.
Afiliação
  • Gleim F; Institut für Anorganische Chemie, Rheinische Friedrich-Wilhelms-Universität Bonn, Gerhardt-Domagk-Straße 1, 53121 Bonn, Germany. r.streubel@uni-bonn.de.
  • Schnakenburg G; Institut für Anorganische Chemie, Rheinische Friedrich-Wilhelms-Universität Bonn, Gerhardt-Domagk-Straße 1, 53121 Bonn, Germany. r.streubel@uni-bonn.de.
  • Ferao AE; Facultad de Química, Campus de Espinardo, Universidad de Murcia, 30100 Murcia, Spain. artuesp@um.es.
  • Streubel R; Institut für Anorganische Chemie, Rheinische Friedrich-Wilhelms-Universität Bonn, Gerhardt-Domagk-Straße 1, 53121 Bonn, Germany. r.streubel@uni-bonn.de.
Chem Commun (Camb) ; 60(19): 2625-2628, 2024 Feb 29.
Article em En | MEDLINE | ID: mdl-38334361
ABSTRACT
Herein, we describe the synthesis of a 1,2σ3λ3-oxaphosphetane from ethylene oxide and its reactions with alkyl halides to form ß-halo phosphane oxides in an Arbuzov-type reaction. When methyl triflate was used as a hard electrophile, cationic oligomerisation of 1,2-oxaphosphetanes was observed. DFT calculations indicate 1,2-oxaphosphetan-2-iums as intermediates and reveal differences between the Arbuzov and the potential Perkow reaction pathway.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Chem Commun (Camb) Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Chem Commun (Camb) Ano de publicação: 2024 Tipo de documento: Article