Construction of 4-substituted 2-(pyrrolidine-3-yl)acetic acid derivatives as cyclic γ-aminobutyric acid analogues employing intermolecular [2+2]-photocycloaddition as key steps
-
Add time:07/13/2019 Source:sciencedirect.com
The synthesis of new 2-(pyrrolidine-3-yl)acetic acid derivatives as cyclic γ-aminobutyric acid analogues, which are additionally substituted at the 4-position, is reported. A de Mayo reaction, i.e. a combination of an intermolecular [2+2]-photocycloaddition of 1,3-dioxinones with N-protected 3-pyrroline and a fragmentation reaction of the resulting cyclobutane moiety, represent the key steps.
We also recommend Trading Suppliers and Manufacturers of 2-aMino-2-(pyrrolidin-3-yl)acetic acid (cas 1214812-00-6). Pls Click Website Link as below: cas 1214812-00-6 suppliers
Prev:Novel routes to either racemic or enantiopure α-amino-(4-hydroxy-pyrrolidin-3-yl)acetic acid derivatives and biological evaluation of a new promising pharmacological scaffold
Next:Farnesol induces fatty acid oxidation and decreases triglyceride accumulation in steatotic HepaRG cells) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Novel routes to either racemic or enantiopure α-amino-(4-hydroxy-pyrrolidin-3-yl)acetic acid derivatives and biological evaluation of a new promising pharmacological scaffold07/12/2019
- Development of selective inhibitors for the treatment of rheumatoid arthritis: (R)-3-(3-(Methyl(7H-pyrrolo[2,3-d]pyrimidin-4-yl)amino)pyrrolidin-1-yl)-3-oxopropanenitrile as a JAK1-selective inhibitor07/11/2019
-
Health and Chemical more >


