Zinc or indium-mediated Barbier-type allylation of aldehydes with 3-bromomethyl-5H-furan-2-one in aqueous media: an efficient synthesis method for α-methylene-γ-butyrolactone
| Autor: | Yu‐Zhe Gao, Xue Wang, Li‐Dong Sun, Xiaohua Xu, Longguan Xie |
|---|---|
| Rok vydání: | 2012 |
| Předmět: |
Aldehydes
Aqueous solution Molecular Structure Organic Chemistry Enantioselective synthesis Diastereomer α methylene γ butyrolactone chemistry.chemical_element Zinc Indium Biochemistry 3-bromomethyl-5H-furan-2-one 4-Butyrolactone chemistry Solvents Molecule Organic chemistry Physical and Theoretical Chemistry Furans |
| Zdroj: | Organic & Biomolecular Chemistry. 10:3991 |
| ISSN: | 1477-0539 1477-0520 |
| Popis: | A zinc or indium-mediated Barbier-type allylation of aldehydes with 3-bromomethyl-5H-furan-2-one in aqueous solvents was developed to provide an efficient route to α-methylene-γ-butyrolactone, which is synthetically very useful. The desired products were obtained in moderate to high yields in aqueous solvents. Excellent drs were achieved, among which the best diastereomeric ratios of products were found when water was used in the indium-mediated reaction, and THF-NH(4)Cl (sat, aq) (2 : 1) mixture in the zinc-mediated reaction. Furthermore, the allylation can be induced by chiral centers, especially those in the α-position, as a substrate-controlled reaction to obtain the enantioselective homoallylation alcohols. |
| Databáze: | OpenAIRE |
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