96854-24-9

Usage

Uses

Used in Biochemical Research:
N-(Methoxycarbonyl)-L-serine Methyl Ester is used as a key building block for the synthesis of complex carbohydrates and glycoconjugates, which are essential for understanding the structure and function of various biological systems.
Used in Pharmaceutical Industry:
N-(Methoxycarbonyl)-L-serine Methyl Ester is used as a synthetic precursor for the production of therapeutic agents, particularly those targeting carbohydrate-related diseases and disorders.
Used in the Synthesis of Tn Antigen:
N-(Methoxycarbonyl)-L-serine Methyl Ester is used as a crucial component in the synthesis of Tn antigen (GalNAc-α-O-Ser), which possesses significant biological properties and is involved in various cellular processes, including cell adhesion, immune response, and cell signaling.

Upstream product

• 186581-53-3 diazomethane 
• 2788-84-3 (S)-serine methyl ester 
• 79-22-1 methyl chloroformate 
• 5680-80-8 methyl (2S)-2-amino-3-hydroxypropanoate hydrochloride 
• 2104-89-4 D-serine methyl ester 

Downstream Products

• 141943-22-8 (R)-4-(2,3-Dimethoxy-phenyl)-2-methoxycarbonylamino-butyric acid 
• 141943-22-8 (S)-4-(2,3-Dimethoxy-phenyl)-2-methoxycarbonylamino-butyric acid 
• 141943-20-6 (R)-2,2-Dimethyl-4-((S)-3,3,3-trifluoro-2-methoxy-2-phenyl-propionyloxymethyl)-oxazolidine-3-carboxylic acid methyl ester 
• 5680-80-8 methyl (2S)-2-amino-3-hydroxypropanoate hydrochloride 
• 96854-27-2 (R)-<2-(Methoxycarbonyl)-2-<(methoxycarbonyl)amino>ethyl>triphenylphosphonium Iodide 
• 147671-72-5 [(S)-1-(tert-Butyl-dimethyl-silanyloxymethyl)-2-(tert-butyl-diphenyl-silanyloxy)-ethyl]-carbamic acid methyl ester 

Relevant academic research and scientific papers

Process for a phenylthiobutyl-isoquinoline and intermediates therefor

The present invention relates to a new method for making compounds of formula and intermediates for making compounds of formual II. The compounds of this invention are useful intermediates for the manufacture of pharmacologically active compounds suitable

Stereocontrolled Construction of Substituted Pyrrolidines based on Intramolecular Protodesilylation Reaction. Enantiospecific Synthesis of (-)-Kainic Acid and (+)-Allokainic Acid from L-Serine

Novel stereocontrolled enantiospecific syntheses of (-)-kainic acid and (+)-allokainic acid have been achieved starting from L-serine via two modes of C-2 and C-3 side chain-directed intramolecular protodesilylations of 4-(trimethylsilylmethyl)ethylidenepyrrolidines.

Enantiospecific synthesis of R- and S-5,6-dihydroxy-2-(N,N-di-n-propylamino)tetralins from serine

The first enantiospecific synthesis of 5,6-dihydroxy-2-(N,N-di-n-propylamino)tetralin [5,6-(HO)2DPAT] is reported. Starting from D- or L-serine either enantiomer is readily available in high optical purity.

Synthesis and absolute configuration of wybutine, the fluorescent minor base from phenylalanine transfer ribonucleic acids

The phosphonium chloride 6 having an optically active amino acid moiety was synthesized from (S)-serine benzyl ester tosylate (2b) through a six-step route. The utility of 6 as a reagent for the Wittig reaction was exemplified in the olefination with benz