2002
DOI: 10.1016/s0040-4020(01)01229-7
|View full text |Cite
|
Sign up to set email alerts
|

Lewis acid catalyzed acylation reactions: scope and limitations

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1

Citation Types

1
57
0

Year Published

2003
2003
2017
2017

Publication Types

Select...
6
3

Relationship

0
9

Authors

Journals

citations
Cited by 140 publications
(61 citation statements)
references
References 36 publications
1
57
0
Order By: Relevance
“…In fact, allyl, cinnamyl and propargyl alcohols were subjected as unsaturated alcohols. We would have expected to carry out hydration reaction on double and triple bond in acidic media beside acetylation reaction, so far hydrated products didn't observed at all (entries [16][17][18]. Heterocyclic furfuryl alcohol gives corresponding acetate with excellent yield (entries 26).…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…In fact, allyl, cinnamyl and propargyl alcohols were subjected as unsaturated alcohols. We would have expected to carry out hydration reaction on double and triple bond in acidic media beside acetylation reaction, so far hydrated products didn't observed at all (entries [16][17][18]. Heterocyclic furfuryl alcohol gives corresponding acetate with excellent yield (entries 26).…”
Section: Resultsmentioning
confidence: 99%
“…6 Commonly used reagent for this reaction uses acetic anhydride in the presence of an acid or base catalyst. 16 and Bi(OTf) 3 , 17 have been investigated to meet the demands for more efficient and selective methods. In spite of these waves of interest, due to the importance of acetylation, it is necessary to develop inexpensive, ecofriendly and reusable catalyst to promote acetylation process.…”
Section: Introductionmentioning
confidence: 99%
“…26,27 In conclusion, we have shown that Al(HSO 4 ) 3 is a good reagent for acetylation and formylation of a variety of alcohols under mild reaction conditions. The reactions are clean and the products yields are good to high and the procedure is easy.…”
mentioning
confidence: 76%
“…Regioselective acetylation is one of the strategies that chemists have tentatively developed, over time, in order to maximize the different reactivity of the primary hydroxyl groups in polyols and carbohydrates to be used as constituents of many biologically active compounds [1][2][3][4]. In the literature, several methods have been developed for the preparation of acetyl derivatives, using zeolites [5], various metal salts such as Mg(ClO 4 ) 2 and Zn(ClO 4 ) 2 .6H 2 O [6,7], and some triflate catalysts or stoichiometric reagents [8,9].…”
Section: Introductionmentioning
confidence: 99%