Stereoselective synthesis of (E)-β-arylvinyl bromides by microwave-induced reaction of anti-3-aryl-2,3-dibromopropanoic acids using an AgOAc–AcOH system
-
Add time:07/31/2019 Source:sciencedirect.com
(E)-β-Arylvinyl bromides were stereoselectively prepared in high yields by microwave irradiation of the corresponding anti-3-aryl-2,3-dibromopropanoic acids in AcOH in the presence of AgOAc for 0.5–3.0 min.
We also recommend Trading Suppliers and Manufacturers of 2-broMo-3-oxo-3-phenylpropanoic acid (cas 132089-31-7). Pls Click Website Link as below: cas 132089-31-7 suppliers
Prev:Strecker aldehydes and α-keto acids, produced by carbonyl–amine reactions, contribute to the formation of acrylamide
Next:The preparation and alkylation of a butanedione-derived chiral glycine equivalent and its use for the synthesis of α-amino acids and α,α-disubstituted amino acids) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- The preparation and alkylation of a butanedione-derived chiral glycine equivalent and its use for the synthesis of α-amino acids and α,α-disubstituted amino acids08/01/2019
- Strecker aldehydes and α-keto acids, produced by carbonyl–amine reactions, contribute to the formation of acrylamide07/30/2019
- Grinding assisted, column chromatography free decarboxylative carbon-carbon bond formation: Greener synthesis of 3, 3-disubstituted oxindoles07/29/2019
- Chemoenzymatic synthesis of both enantiomers of 3-hydroxy- and 3-amino-3-phenylpropanoic acid07/28/2019
-
Health and Chemical more >