AI Article Synopsis
- A new protocol was created for synthesizing α-amino-vinylphosphine oxides using a reaction between alkyl nitriles and phosphine oxides.
- The reaction is efficiently catalyzed by a combination of manganese acetate (Mn(OAc), a Lewis acid) and guanidine (a Lewis base).
- This method allows for various alkyl nitriles and phosphine oxides to be used, achieving product yields of up to 95% under mild conditions, and it is suitable for gram-scale production.
Article Abstract
A protocol for the synthesis of α-amino-vinylphosphine oxides by phosphinoenamination reaction between alkyl nitriles and phosphine oxides was developed. The combination of Mn(OAc) as a Lewis acid and guanidine as a Lewis base was found to be an efficient catalytic system for this reaction. A series of alkyl nitriles and phosphine oxides are compatible with this conversion, furnishing the desired products in up to 95% yield under mild conditions. Furthermore, this method demonstrates the capability of gram-scale synthesis.
Download full-text PDF |
Source |
|---|---|
| http://dx.doi.org/10.1039/d4ob00489b | DOI Listing |
Publication Analysis
Top Keywords
alkyl nitriles
12
synthesis α-amino-vinylphosphine
8
α-amino-vinylphosphine oxides
8
nitriles phosphine
8
phosphine oxides
8
efficient synthesis
4
oxides
4
oxides alkyl
4
nitriles manganese-catalyzed
4
manganese-catalyzed phosphinoenamination
4
Similar Publications
Want AI Summaries of new PubMed Abstracts delivered to your In-box?
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!