Synthesis of , of α,β-unsaturated aldehydes and nitriles via cross-metathesis reactions using Grubbs’ catalysts
Data(s) |
22/09/2014
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Resumo |
<p>A series of alpha,beta-unsaturated aldehydes and nitriles of significant interest in the fragrance industry have been prepared using Grubbs' catalysts in cross-metathesis reactions of electron-deficient olefins (i.e., acrolein, crotonaldehyde, methacrolein, and acrylonitrile) with various 1-alkenes, including 1-decene, 1-octene, 1-hexene and 2-allyloxy-6-methylheptane. The latter is of particular interest, as it has not previously being used as a substrate in cross-metathesis reactions and allows access to valuable intermediates for the synthesis of new fragrances. Most reactions gave good selectivity of the desired CM product (>= 90%). Detailed optimisation and mechanistic studies have been performed on the cross-metathesis of acrolein with 1-decene. Recycling of the catalyst has been attempted using ionic liquids. </p> |
Identificador | |
Idioma(s) |
eng |
Direitos |
info:eu-repo/semantics/restrictedAccess |
Fonte |
Rountree , S M , Taylor , S F R , Hardacre , C , Lagunas , M C & Davey , P N 2014 , ' Synthesis of , of α,β-unsaturated aldehydes and nitriles via cross-metathesis reactions using Grubbs’ catalysts ' Applied Catalysis A: General , vol 486 , pp. 94-104 . DOI: 10.1016/j.apcata.2014.08.032 |
Palavras-Chave | #Cross-metathesis #Grubbs' catalysts #Acrolein #Fragrances #FATTY-ACID DERIVATIVES #HETEROCYCLIC CARBENE LIGANDS #SELECTIVE OLEFIN METATHESIS #TEMPERATURE IONIC LIQUIDS #QUATERNARY AMMONIUM GROUP #RING-CLOSING METATHESIS #DIELS-ALDER REACTIONS #METHYL ACRYLATE #UNSATURATED ALDEHYDES #RUTHENIUM CATALYSTS #/dk/atira/pure/subjectarea/asjc/1600 #Chemistry(all) |
Tipo |
article |