143293-00-9

Upstream product

• 13734-34-4 N-tert-butoxycarbonyl-L-phenylalanine 
• 133489-81-3 1,1-dimethylethyl (S)-<1-(cyclohexylmethyl)-2-(2-furanyl)-2-oxoethyl>carbamate 
• 115766-13-7 (S)-α-[[(1,1-dimethylethoxy)carbonyl]amino]-N-methoxy-N-methylcyclohexanepropanamide 
• 98105-42-1 (S)-2-(t-butoxycarbonylamino)-3-cyclohexyl-1-propanal 
• 133660-33-0 (4S-trans)-4-(cyclohexylmethyl)-5-(2-furanyl)-2-oxazolidinone 

Downstream Products

• 150593-82-1 <4S-<4α,5β(S^*)>>-5-(4-bromo-1-hydroxybutyl)-4-cyclohexylmethyl-2-oxazolidinone 
• 150593-84-3 Thioacetic acid S-[(R)-4-((4S,5R)-4-cyclohexylmethyl-2-oxo-oxazolidin-5-yl)-4-methanesulfonyloxy-butyl] ester 
• 150593-83-2 2-carboxyamino-1-cyclohexyl-1,2,5,6-tetradeoxy-7-thio-D-xylo-heptitol-7-acetate, intramol-2,3-ester 
• 150593-85-4 2-carboxamino-1-cyclohexyl-1,2,4,5,6,7-hexadeoxy-4,7-epithio-L-arabino-heptitol, intramol-2,3-ester 

Relevant academic research and scientific papers

THE SYNTHESIS OF HETEROCYCLIC C-TERMINAL UNITS WHICH MIMIC THE TRANSITION STATE IN THE CLEAVAGE OF THE LEU-VAL BOND OF ANGIOTENSINOGEN BY RENIN

The stereospecific synthesis of (S)2-amino-3-cyclohexyl-(R)1-(2-furanyl)-propan-1-ol (17) and (S)2-amino-3-cyclohexyl-(R)1-(2-thienyl)-propan-1-ol (18) from t-Boc-L-phenylalanine is described.Reduction of the furan ring of (4S-trans)-4-(cyclohexylmethyl)-