Synthesis of new pyrrolidine-1,2-dicarboxamides and investigation of their activity for the synthesis of aminonitriles was written by Aydin, Ozge;Yolacan, Cigdem;Aydogan, Feray. And the article was included in American Chemical Science Journal in 2016.Recommanded Product: 5856-63-3 This article mentions the following:
New pyrrolidine-1,2-dicarboxamide derivatives were synthesized by the amidation reactions of some amines, an amino alc. and an amino acid ester with (S)-1-(phenylcarbamoyl)pyrrolidine-2-carboxylic acid, which was obtained by the reaction of L-proline with Ph isocyanate. Activities of these compounds for the synthesis of aminonitriles via Strecker reaction were investigated. The aminonitriles were obtained in good yields; however, no significant asym. induction was observed In the experiment, the researchers used many compounds, for example, (R)-2-Aminobutan-1-ol (cas: 5856-63-3Recommanded Product: 5856-63-3).
(R)-2-Aminobutan-1-ol (cas: 5856-63-3) belongs to alcohols. Because alcohols are easily synthesized and easily transformed into other compounds, they serve as important intermediates in organic synthesis. Under carefully controlled conditions, simple alcohols can undergo intermolecular dehydration to give ethers. This reaction is effective only with methanol, ethanol, and other simple primary alcohols.Recommanded Product: 5856-63-3
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts