134786-33-7

Upstream product

• 134786-21-3 N-tosyl-2-azaspiro<4,5>decane-3-methanol 
• 81097-22-5 N-((1-allylcyclohexyl)methyl)-4-methylbenzenesulfonamide 
• 67838-02-2 methyl 1-allylcyclohexane-1-carboxylate 
• 72335-83-2 1-allylcyclohexane-1-carboxylic acid chloride 
• 72335-77-4 1-Allyl-cyclohexanecarboxylic acid amide 
• 81097-43-0 1-allyl-1-(aminomethyl)cyclohexane 
• 72335-50-3 1-(1-prop-2-enyl)cyclohexanecarboxylic acid 
• 4630-82-4 methyl cyclohexylcarboxylate 

Downstream Products

• 134786-29-1 N-tosyl-α,α-dimethyl-2-azaspiro<4,5>decane-3-methanol 

Relevant academic research and scientific papers

Br?nsted acid-assisted intramolecular aminohydroxylation of N -alkenylsulfonamides under heavy metal-free conditions

The intramolecular aminohydroxylation of N-alkenylsulfonamides proceeded under heavy metal-free conditions to give substituted prolinol derivatives in high yields. Oxone activated by catalytic Br?nsted acid worked well as an electrophilic oxidant for this reaction.

CYCLISATION DE N-TOSYL OXIRANES-PROPYLAMINES: SYNTHESE D'HETEROCYCLES AZOTES.

The cyclisation of N-tosyl-oxiranepropylamines is accomplished in aqueous basic medium and in anhydrous acid medium as well.In most cases, this reaction occurs by a regiospecific 5-exo-tet. ring closure and affords N-tosyl-2-pyrrolidinemethanols in high y