One-pot synthesis and theoretical calculation for trifluoromethylated pyrrolizidines by 1,3-dipolar cycloaddition with azomethine ylides and β-trifluoromethyl acrylamides
-
Add time:08/30/2019 Source:sciencedirect.com
The reaction with β-trifluoromethyl acrylamide 3e and azomethine ylides generated from l-proline and several aldehydes provided the corresponding trifluoromethylated pyrrolizidines with excellent diastereoselectivity (>20/1) in all cases and moderate regioselectivity (up to 1/5.9). A DFT calculation was also examined to reveal the origin of these stereoselectivities.
We also recommend Trading Suppliers and Manufacturers of 2-METHOXY-4-(TRIFLUOROMETHYL)BENZALDEHYDE (cas 132927-09-4). Pls Click Website Link as below: cas 132927-09-4 suppliers
Prev:Facile synthesis of aromatic unsymmetrical fluorine-containing acyloins through the reductive trifluoroacetylation of benzaldehyde and transposition of the carbonyl group
Next:Detection and quantification of 4-hydroxy-1-(3-pyridyl)-1-butanone (HPB) from smoker albumin and its potential as a surrogate biomarker of tobacco-specific nitrosamines exposure and bioactivation) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Facile synthesis of aromatic unsymmetrical fluorine-containing acyloins through the reductive trifluoroacetylation of benzaldehyde and transposition of the carbonyl group08/29/2019
- Access to substituted trifluoromethyl ketones using the versatile synthetic intermediate (E)-1,1-dimethyl-2-(1,1,1-trifluoropropan-2-ylidene)hydrazine08/28/2019
- Synthesis and biological evolution of hydrazones derived from 4-(trifluoromethyl)benzohydrazide08/27/2019
-
Health and Chemical more >
-
Related Products


