170157-64-9

Usage

Uses

Boc-beta-(2-quinolyl)-d-ala-oh

Upstream product

• 123-91-1 1,4-dioxane 
• 210420-41-0 N-Acetyl-β-(2-quinolyl)-L-alanine 
• 24424-99-5 di-tert-butyl dicarbonate 
• 161453-32-3 (2S,5S)-(+)-5-(2'-quinolylmethyl)-2-tert-butyl-1-tert-butoxycarbonyl-3-methyl-4-imidazolidinone 
• 161513-46-8 (S)-(+)-2-amino-3-(2'-quinolyl)propionic acid 

Relevant academic research and scientific papers

Boronic ester and acid compounds, synthesis and uses

Disclosed herein are boronic ester and acid compounds, their synthesis and uses. More specifically, disclosed herein is a method for reducing the rate of degradation of proteins in an animal comprising contacting cells of the animal with certain boronic ester and acid compounds.

BORONIC ESTER AND ACID COMPOUNDS

Disclosed herein is a method for reducing the rate of degradation of proteins in an animal comprising contacting cells of the animal with certain boronic ester and acid compounds. Also disclosed herein are novel boronic ester and acid compounds, their synthesis and uses.

Intercalator amino acids: Synthesis of heteroaryl alanines

Stereoselective alkylation of (S)-(-)-2-t-butyl-1-t-butyloxycarbonyl-3-methyl-4-imidazolinone with 2-chloromethylquinoline, 2-chloromethylquinoxaline and 5-chloromethyl-1,10-phenanthroline, followed by hydrolysis, afforded the corresponding (S)-(+)-α-amino acids with high enantiomeric excess.