1315471-19-2

Upstream product

• 115977-54-3 trans-2-hexenyl iodide 
• 223526-27-0 (4S,4''S)-4-<3'-(4''-benzyl-2''-oxo-oxazolidin-3''-yl)-3'-oxo-propyl>-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester 
• 90719-32-7 (S)-4-Benzyl-2-oxazolidinone 
• 223526-25-8 (4S)-4-(2'-carboxyethyl)-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester 

Downstream Products

• 1315471-23-8 C₂₆H₄₁NO₆S 

Relevant academic research and scientific papers

An improved synthesis of (2S, 4S)- and (2S, 4R)-2-amino-4-methyldecanoic acids: Assignment of the stereochemistry of culicinins

An improved synthesis of (2S, 4S)- and (2S, 4R)-2-amino-4-methyldecanoic acids was accomplished using a glutamate derivative as starting material and Evans' asymmetric alkylation as the decisive step. The NMR data of the two diastereomers were measured and compared with those of the natural product. As a result, the stereochemistry of this novel amino acid unit in culicinins was assigned as (2S, 4R).