87635-86-7

Upstream product

• 87635-86-7 trans-2-(1-But-3-enyl)-4-tert-butylcyclohexanone 
• 58911-63-0 4-tert-butylcyclohexanone dimethylhydrazone 
• 5162-44-7 1-bromo-4-butene 

Downstream Products

• 87635-86-7 cis-2-(1-But-3-enyl)-4-tert-butylcyclohexanone 
• 87635-87-8 (2α,4aα,5β,7aα)-2-tert-Butyl-4a-hydroxy-5-methylbicyclo<4.3.0>nonane 
• 87635-87-8 (2α,4aα,5α,7aα)-2-tert-Butyl-4a-hydroxy-5-methylbicyclo<4.3.0>nonane 
• 117874-14-3 c-2-(1-But-3-enyl)-t-4-tert-butylcyclohexanol 
• 117874-06-3 c-2-(1-But-3-enyl)-c-4-phenylcyclohexanol 
• 117874-14-3 c-4-tert-Butyl-t-2-(1-but-3-enyl)cyclohexanol 
• 117874-14-3 c-2-(1-But-3-enyl)-c-4-tert-butylcyclohexanol 
• 117874-09-6 (2α,4aβ,5β,7aβ)-5-Methyl-2-phenylbicyclo<4.3.0>nonane 
• 117874-09-6 (2α,4aβ,5α,7aβ)-5-Methyl-2-phenylbicyclo<4.3.0>nonane 

Relevant academic research and scientific papers

Stereocontrol in a combined allylic azide rearrangement and intramolecular schmidt reaction

Pre-equilibration of an interconverting set of isomeric allylic azides is coupled with an intramolecular Schmidt reaction to afford substituted lactams stereoselectively. The effect of substitution and a preliminary mechanistic study are reported. The syn