Novel complexes between methyltrioxorhenium (MTO) and bis(fluorous- ponytailed) 2,2′bipyridines (bpy-Fn) were synthesized and used for the oxidation of alkenes with hydrogen peroxide under fluorous catalysis. High conversions and yields of the corresponding epoxides were obtained.

Saladino, R., Ginnasi, M., Collalto, D., Bernini, R., Crestini, C. (2010). An Efficient and Selective Epoxidation of Olefins with Novel Methyltrioxorhenium/(Fluorous Ponytailed) 2,2′-Bipyridine Catalysts. ADVANCED SYNTHESIS & CATALYSIS, 352(8), 1284-1290 [10.1002/adsc.201000032].

An Efficient and Selective Epoxidation of Olefins with Novel Methyltrioxorhenium/(Fluorous Ponytailed) 2,2′-Bipyridine Catalysts

CRESTINI, CLAUDIA
2010-01-01

Abstract

Novel complexes between methyltrioxorhenium (MTO) and bis(fluorous- ponytailed) 2,2′bipyridines (bpy-Fn) were synthesized and used for the oxidation of alkenes with hydrogen peroxide under fluorous catalysis. High conversions and yields of the corresponding epoxides were obtained.
2010
Pubblicato
Rilevanza internazionale
Articolo
Sì, ma tipo non specificato
Settore CHIM/03 - CHIMICA GENERALE E INORGANICA
Settore CHIM/06 - CHIMICA ORGANICA
Settore CHIM/08 - CHIMICA FARMACEUTICA
English
Con Impact Factor ISI
L'articolo è disponibile sul sito dell'editore: http://www.onlinelibrary.wiley.com
Saladino, R., Ginnasi, M., Collalto, D., Bernini, R., Crestini, C. (2010). An Efficient and Selective Epoxidation of Olefins with Novel Methyltrioxorhenium/(Fluorous Ponytailed) 2,2′-Bipyridine Catalysts. ADVANCED SYNTHESIS & CATALYSIS, 352(8), 1284-1290 [10.1002/adsc.201000032].
Saladino, R; Ginnasi, M; Collalto, D; Bernini, R; Crestini, C
Articolo su rivista
File in questo prodotto:
File Dimensione Formato  
AdvSynthCatal 352 (2010) 1284-1290Cover.pdf

accesso aperto

Dimensione 122.62 kB
Formato Adobe PDF
122.62 kB Adobe PDF Visualizza/Apri

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/14262
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 12
  • ???jsp.display-item.citation.isi??? 8
social impact