87601-68-1

Upstream product

• 327-57-1 L-Norleucine 
• 21754-55-2 L-norleucine methyl ester 
• 80696-29-3 (S)-(+)-2-Amino-1-hexanol 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 1161012-73-2 (S)-3-tosylamino-heptane-1-nitrile 
• 1161012-67-4 (S)-1-azido-2-tosylamino-hexane 
• 101689-10-5 (S)-3,3,3-Trifluoro-2-methoxy-N-((R)-1-methyl-pentyl)-2-phenyl-propionamide 
• 101689-10-5 3,3,3-Trifluoro-2-methoxy-N-((R)-1-methyl-pentyl)-2-phenyl-propionamide 
• 81329-98-8 4-Methyl-N-((R)-1-methyl-pentyl)-benzenesulfonamide 

Relevant academic research and scientific papers

Synthesis and biological evaluation of reversible inhibitors of IdeS, a bacterial cysteine protease and virulence determinant

Analogues of the irreversible protease inhibitors TPCK and TLCK have been synthesized and tested as inhibitors of the bacterial cysteine protease IdeS excreted by Streptococcus pyogenes. Eight compounds were identified as inhibitors of IdeS in an in vitro

SYNTHESIS OF THE RACEMIC FORM OF (Z)-1,17-DIAMINOOCTADEC-9-ENE, AN ALIPHATIC DIAMINE FROM COCCINELLIDAE. DETERMINATION OF THE ABSOLUTE CONFIGURATION OF THE (+)-NATURALLY-OCCURRING ANTIPODE

The total synthesis of the title compound (1) has been achieved.Also reported is the use of lanthanide induced shifts in 1H NMR spectroscopy to assign the absolute configuration of the α-carbon atom in chiral primary α-methylalkylamines.Application of this empirical method to natural (+)-1 shows that it has the R-configuration at C-17.