27844-10-6

Upstream product

• 996-50-9 N,N-diethyl-1,1,1-trimethylsilanamine 
• 59-51-8 DL-methionine 
• 7677-24-9 trimethylsilyl cyanide 
• 63-68-3 L-methionine 
• 75-77-4 chloro-trimethyl-silane 

Downstream Products

• 5840-77-7 DL-methionine N-carboxyanhydride 
• 79137-57-8 N-Mesitoyl-DL-methionin 
• 79137-65-8 2-Mesityl-4-<2-(methylthio)ethyl>-2-oxazolin-5-on 
• 79137-86-3 N-Mesitoyl-α-(3-oxobutyl)methionin 
• 79137-87-4 N-Mesitoyl-α-(2-cyanethyl)methionin 
• 99744-41-9 N-<2-(Triphenylphosphonio)isopropyloxycarbonyl>-L-methionin-chlorid 
• 86050-11-5 N-<2-(Triphenylphosphonio)ethoxycarbonyl>threonyl-N⁶,N⁶-phthaloyllysyl-methionyl-serin-chlorid 
• 86040-65-5 N-<2-(Triphenylphosphonio)ethoxycarbonyl>methionyl-O-tert-butylserin-tert-butylester-chlorid 
• 86050-09-1 N-<2-(Triphenylphosphonio)ethoxycarbonyl>methionyl-serin-chlorid 
• 86040-87-1 N-<2-(Triphenylphophonio)ethoxycarbonyl>methionyl-seryl-N⁴-(2-acetamido-3,4,6-tri-O-acetyl-2-desoxy-β-D-glucopyranosyl)asparagin-benzylester-chlorid 
• 86040-76-8 N-<2-(Triphenylphosphonio)ethoxycarbonyl>threonyl-N⁶,N⁶-phthaloyllysyl-methionyl-O-tert-butylserin-tert-butylester-chlorid 
• 212120-39-3 [(S)-2-(4-Acetoxy-benzyloxycarbonylamino)-4-methylsulfanyl-butyrylamino]-acetic acid allyl ester 
• 212119-83-0 N-[4-(acetoxy)benzyloxycarbonyl]-glycyl-(S-palmitoyl)-L-cysteyl-L-methionyl-glycyl-L-leucyl-L-prolyl-(S-farnesyl)-L-cysteine methyl ester 
• 170892-93-0 (R)-2-{[(S)-1-((S)-2-{2-[(S)-2-(4-Acetoxy-benzyloxycarbonylamino)-4-methylsulfanyl-butyrylamino]-acetylamino}-4-methyl-pentanoyl)-pyrrolidine-2-carbonyl]-amino}-3-((2E,6E)-3,7,11-trimethyl-dodeca-2,6,10-trienylsulfanyl)-propionic acid methyl ester 

Relevant academic research and scientific papers

Chemoenzymatic synthesis of N-Ras lipopeptides

For the study of biological phenomena influenced by the plasma-membrane- bound Ras proteins and other lipidated proteins, characteristic peptides which embody the correct lipid modifications of their parent proteins (palmitoyl thioesters and farnesyl thio

ENANTIOMERIC QUANTIFICATIONS OF AMINO ACIDS THROUGH THEIR Nα-ACYL AMIDES BY GAS CHROMATOGRAPHY.

Apparent separation of 1.1 or higher on Chiralsil Val III can be obtained for Nα-acyl N-alkyl aminoacid amides allowing the use of short capillary gas chromatographic columns.A clean derivatization protocol without racemization is described, proceding through the NCA derivatives that are prepared from "in situ" silylated amino acids with trimethylsilyl cyanide.