881920-87-2

Upstream product

• 80434-59-9 (1R,2S,5R)-2-isopropyl-5-methylcyclohexanecarboxaldehyde 
• 868744-83-6 (R,E)-1-((1R,2S,5R)-2-isopropyl-5-methylcyclohexyl)hex-2-en-1-ol 
• 66703-03-5 trans-1-iodo-1-pentene 

Downstream Products

• 881920-93-0 (S,E)-1-((1R,2S,5R)-2-isopropyl-5-methylcyclohexyl)hex-2-enyl carbamate 
• 868744-91-6 (S,E)-1-((1R,2S,5R)-2-isopropyl-5-methylcyclohexyl)hex-2-en-1-ol 

Relevant academic research and scientific papers

Stereocontrolled formation of amino acids and N-heterocycles bearing a quaternary chiral carbon

Stereocontrolled formation of tertiary or quaternary chiral carbons bearing nitrogen was achieved using the [3,3]-sigmatropic rearrangement of cyanate to isocyanate as a key element. A short and highly selective sequence of reactions, starting from p-ment