81097-18-9

Upstream product

• 81097-42-9 trans-2-(prop-2-enyl)cyclohexylamine 
• 98-09-9 benzenesulfonyl chloride 
• 81097-47-4 N-benzenesulfonyl-7-azabicyclo<4.1.0>heptane 
• 1730-25-2 allylmagnesium bromide 
• 81097-45-2 trans-1-N-benzenesulfonylamino-2-bromocyclohexane 
• 100-64-1 cyclohexanone-oxime 
• 59239-07-5 2-(2'-propenyl)cyclohexanone oxime 
• 120871-61-6 (Z)-allylcyclohexanone oxime 
• 81097-42-9 cis-2-(prop-2-enyl)cyclohexylamine 

Downstream Products

• 120871-63-8 (S)-1-Benzenesulfonyl-octahydro-indol-2-ol 
• 81097-19-0 N-[(1R,2S)-2-(2-Oxo-propyl)-cyclohexyl]-benzenesulfonamide 
• 120871-63-8 (3aS,7aS)-1-Benzenesulfonyl-octahydro-indol-2-ol 
• 120871-37-6 (Z)-7-((1R,2R)-2-Benzenesulfonylamino-cyclohexyl)-hept-5-enoic acid methyl ester 
• 120926-28-5 (Z)-7-((1R,2R)-2-Benzenesulfonylamino-cyclohexyl)-hept-5-enoic acid 
• 120871-37-6 (Z)-7-((1S,2R)-2-Benzenesulfonylamino-cyclohexyl)-hept-5-enoic acid methyl ester 
• 120926-28-5 (Z)-7-((1S,2R)-2-Benzenesulfonylamino-cyclohexyl)-hept-5-enoic acid 

Relevant academic research and scientific papers

SYNTHESIS OF MONOCYCLIC ANALOGUES OF A POTENT THROMBOXANE RECEPTOR ANTAGONIST, (+/-)-(5Z)-7-BICYCLOHEPT-2-EXO-YL>HEPTENOIC ACID (S-145)

Several monocyclic analogues of the potent thromboxane-A2 receptor antagonist S-145, i.e. cyclohexane, cyclopentane, tetrahydrofuran, and pyrrolidine, as well as the biclooctane one were synthesized using allylation via oxime dianion and the Barton's method for oxime reduction in the key steps.

Palladium-Catalyzed Cyclization of ω-Olefinic Tosamides. Synthesis of Nonaromatic Nitrogen Heterocycles

The cyclization of aliphatic amino olefins to nonaromatic nitrogen heterocycles nas been accomplished by conversion of the amine to the corresponding p-toluenesulfonamide, followed by Pd(II)-catalyzed intramolecular amination of the olefin.The resulting t