158414-47-2

Upstream product

• 98-89-5 Cyclohexanecarboxylic acid 
• 16537-05-6 tert-butyl cyclohexanecarboxylate 
• 22173-21-3 tert-butyl cyclohex-1-ene-1-carboxylate 

Downstream Products

• 158414-45-0 (1S,2S)-(+)-2-aminocyclohexane-1-carboxylic acid hydrochloride 
• 158414-49-4 tert-butyl (1S,2S,αS)-2-(N-benzyl-N-α-methylbenzylamino)cyclohexane-1-carboxylate 
• 158414-45-0 (-)-(1R,2S)-2-aminocyclohexanecarboxylic acid hydrochloride 

Relevant academic research and scientific papers

Asymmetric Synthesis of (-)-(1R,2S)-Cispentacin and Related cis- and trans-2-Amino Cyclopentane- and Cyclohexane-1-carboxylic Acids

The antifungal antibiotic (-)-(1R,2S)-2-aminocyclopentane-1-carboxylic acid (cispentacin) 8 and its cyclohexane homologue 14 have been prepared utilizing the highly stereoselective conjugate addition of homochiral lithium N-benzyl-N-α-methylbenzylamide 5.