88611-69-2

Upstream product

• 5153-67-3 nitrostyrene 
• 106-99-0 buta-1,3-diene 
• 77-79-2 3-Sulfolene 
• 102-96-5 (2-nitroethenyl)benzene 

Downstream Products

• 76784-68-4 N-hydroxy-7-phenyl-3H,6H,7H-azepin-2-one 
• 17293-45-7 trans-2-phenylcyclohexylamine 
• 134745-91-8 (+/-)-trans-6-amino-1-phenyl-cyclohexene-⁽³⁾ 
• 17448-50-9 cis-1-nitro-2-phenylcyclohexanone 
• 5554-79-0 (+/-)-1-aci-1-nitro-2-phenyl-cyclohexane 
• 134745-97-4 N-((Z)-2-Iodo-but-2-enyl)-4-methyl-N-((1R,6S)-6-phenyl-cyclohex-3-enyl)-benzenesulfonamide 
• 134745-97-4 N-((E)-2-Iodo-but-2-enyl)-4-methyl-N-((1R,6S)-6-phenyl-cyclohex-3-enyl)-benzenesulfonamide 
• 134745-98-5 (1R,5S,8S)-4-Eth-(E)-ylidene-8-phenyl-2-(toluene-4-sulfonyl)-2-aza-bicyclo[3.3.1]non-6-ene 
• 134745-98-5 (1R,5S,8S)-4-Eth-(Z)-ylidene-8-phenyl-2-(toluene-4-sulfonyl)-2-aza-bicyclo[3.3.1]non-6-ene 
• 134745-94-1 N-(2-Bromo-allyl)-4-methyl-N-((1R,6S)-6-phenyl-cyclohex-3-enyl)-benzenesulfonamide 
• 134745-95-2 (1R,5S,8S)-4-Methylene-8-phenyl-2-(toluene-4-sulfonyl)-2-aza-bicyclo[3.3.1]non-6-ene 
• 134745-93-0 4-Methyl-N-((1S,6R)-6-phenyl-cyclohex-3-enyl)-benzenesulfonamide 
• 134745-92-9 ((1S,6R)-6-Phenyl-cyclohex-3-enyl)-carbamic acid tert-butyl ester 
• 17448-50-9 (+/-)-trans-1-nitro-2-phenyl-cyclohexane 

Relevant academic research and scientific papers

Organocatalytic Michael addition/intramolecular Julia-Kocienski olefination for the preparation of nitrocyclohexenes

An asymmetric organocatalytic [3 + 3] annulation strategy based on a Michael addition/intramolecular Julia-Kocienski olefination sequence has been developed for the synthesis of 4-substituted-5-nitrocyclohex-1-ene compounds. The strategy is an alternative to the direct reluctant enantioselective Diels-Alder approach. The potential of the methodology has been demonstrated with a concise enantioselective formal synthesis of trandolapril.

Structure-activity relationships of phenylcyclohexene and biphenyl antitubulin compounds against plant and mammalian cells

Phenylcyclohexenes (PCHs) [e.g., trans-4-nitro-5-(2,3,4-trimethoxyphenyl)cyclohexene, 2d] were found to bind weakly to the colchicine site of bovine tubulin, but are the first mimics of colchicine found to have high activity towards plant cells. Structure