168126-69-0

Upstream product

• 21087-29-6 trans-3-phenylprop-2-enyl chloride 
• 98-59-9 p-toluenesulfonyl chloride 
• 325490-29-7 (1R)-1-phenylprop-2-en-1-amine 
• 85217-69-2 cinnamyl methyl carbonate 
• 18522-92-4 sodium p-toluenesulfonamide 
• 177171-57-2 (1S,3S,5R,7R)-3-Chloro-10,10-dimethyl-3-((E)-3-phenyl-allyl)-4-oxa-3λ⁴-selena-tricyclo[5.2.1.0^1,5]decane 
• 177171-55-0 (1S,2R,4R)-7,7-Dimethyl-1-((E)-3-phenyl-allylselanylmethyl)-bicyclo[2.2.1]heptan-2-ol 
• 177171-61-8 C₂₆H₃₃NO₃SSe 

Downstream Products

• 1044148-83-5 (R)-1-phenyl-N-((R)-1-phenylallyl)-N-tosylprop-2-en-1-amine 
• 1284206-40-1 4-methyl-N-[(1R)-1-phenylprop-2-en-1-yl]-N-(prop-2-yn-1-yl)benzenesulfonamide 

Relevant academic research and scientific papers

Bicyclic cyclopentenones via the combination of an iridium-catalyzed allylic substitution with a diastereoselective intramolecular pauson-khand reaction

Enantioselective syntheses of bicyclic cyclopentenones are described. Key steps are an iridium-catalyzed allylic substitution and an intramolecular diastereoselective Pauson-Khand reaction. The diastereoselectivity of the Pauson-Khand reaction was found t

A novel access to tetrahydro-β-carbolines via one-pot hydroformylation/fischer indole synthesis: Rearrangement of 3,3- spiroindoleninium cations

(Chemical Equation Presented) The two component one-pot hydroformylation/Fischer indole synthesis sequence of 2,5 dihydropyrroles and phenyl hydrazines allows a facile and convenient access to tetrahydro-β- carbolines in moderate to good yields.