881920-82-7

Upstream product

• 881920-78-1 (1S,2S,4R)-2-((R,E)-3-isocyanato-3-methylhex-1-enyl)-1-isopropyl-4-methylcyclohexane 
• 24324-17-2 9-Fluorenylmethanol 
• 881920-66-7 (S,E)-1-((1R,2S,5R)-2-isopropyl-5-methylcyclohexyl)-3-methylhex-2-en-1-ol 
• 142921-16-2 (E)-1-iodo-2-methylpent-1-ene 
• 881920-72-5 (S,E)-1-((1R,2S,5R)-2-isopropyl-5-methylcyclohexyl)-3-methylhex-2-enyl carbamate 

Downstream Products

• 920749-77-5 (R)-1-[(E)-2-((1S,2S,5R)-2-Isopropyl-5-methyl-cyclohexyl)-vinyl]-1-methyl-butylamine 
• 920749-79-7 But-3-enyl-{(R)-1-[(E)-2-((1S,2S,5R)-2-isopropyl-5-methyl-cyclohexyl)-vinyl]-1-methyl-butyl}-amine 

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

Cleavage of a chiral auxiliary using RCM on an especially sterically crowded alkene: Syntheses of chiral carbo- and heterocycles

Chiral 1,5-, 1,6-, and 1,7-dienes generated in 3-4 steps from chiral auxiliary p-menthane-3-carboxaldehyde undergo RCM with notable discrepancies in reactivity depending on the nature and number of substituents flanking the central double bond. The chiral