129397-39-3

Upstream product

• 19810-31-2 Benzyloxyacetyl chloride 
• 129397-36-0 N-(2-cyclohexylethylidene)-(S)-α-methylbenzylamine 
• 139007-45-7 S-(2-Pyridyl) 2-(phenylmethoxy)ethanethioate 
• 129397-36-0 [2-Cyclohexyl-eth-(E)-ylidene]-((S)-1-phenyl-ethyl)-amine 

Downstream Products

• 129397-43-9 isopropyl (2R,3S)-2-benzyloxy-4-cyclohexyl-3-<(S)-(1-phenylethyl)amino>butyrate 
• 141280-91-3 isopropyl (2R,3S)-3-acetamido-2-acetoxy-4-cyclohexylbutyrate 
• 121506-22-7 (2R,3S)-nor-C-statine hydrochloride 
• 119642-26-1 2(R)-hydroxy-3(S)-amino-4-cyclohexylbutanoic acid 2-propyl ester 

Relevant academic research and scientific papers

Stereoselective synthesis of β-lactams by condensation of titanium enolates of 2-pyridyl thioesters with imines bearing a chiral auxiliary

Several amines have been tested as chiral auxiliaries in the stereoselective synthesis of β-lactams by condensation of the titanium enolates of 2-pyridyl thioesters with chiral imines. The amines were selected among the following classes of compounds: ben

A NOVEL SYNTHESIS OF CYCLOHEXYLNORSTATINE ISOPROPYL ESTER, THE C-TERMINAL COMPONENT OF A RENIN INHIBITOR

The title compound was produced diastereoselectively in racemic and optically active forms by employing the cycloaddition reaction of an imine with benzyloxyketene followed by acidic alcoholysis of the formed 3,4-cis-disubstituted β-lactam with isopropanol.