Réactions d'acylation sous irradiation micro-onde. II. Acylation d'éthers aromatiques

Laporte, Christian; Marquié, Julien; Laporterie, A.; Desmurs, Jean‐Roger; Dubac, J.

doi:10.1016/s1387-1609(00)88560-6

Cited by 11 publications

(30 citation statements)

References 19 publications

Supporting

Mentioning

Contrasting

Order By: Relevance

“…Scheme 25 The Bi(OTf) 3 -catalysed benzoylation of anisole under microwave (MW) irradiation led without temperature control to shorter reaction times due to the specific interaction of MW with the produced aryl ketone and especially with the catalystϪketone complex (Scheme 26). [53] Scheme 26…”

Section: Acylation Reactionsmentioning

confidence: 99%

Bismuth(III) Triflate in Organic Synthesis

2004

View full text Add to dashboard Cite

show abstract

Section: Acylation Reactionsmentioning

confidence: 99%

Bismuth(III) Triflate in Organic Synthesis

2004

View full text Add to dashboard Cite

show abstract

“…Solvent-free benzoylation of aromatic ethers has been performed under the action of microwave irradiation in the presence of a metallic catalyst, FeCl 3 being one of the most efficient [101]. With careful control of the temperature and other parameters, nonthermal microwave effects have not been observed either in terms of yields or isomeric ratios of the obtained products (Eq.…”

Section: Friedel±crafts Acylation Of Aromatic Ethersmentioning

confidence: 99%

Nonthermal Effects of Microwaves in Organic Synthesis

Perreux¹,

Loupy²

2002

Microwaves in Organic Synthesis

View full text Add to dashboard Cite

“…Solvent-free benzoylation of aromatic ethers has been performed under the action of MW irradiation in the presence of a metallic catalyst, FeCl 3 being one of the most efficient [197]. The reactive species is the acylium ion resulting from abstraction of a chloride anion from benzoyl chloride [Eq.…”

Section: Friedel-crafts Acylation Of Aromatic Ethersmentioning

confidence: 99%