1255767-99-7

Upstream product

• 87802-78-6 dimethyl (S)-2-(1-phenylallyl)malonate 
• 106-96-7 propargyl bromide 

Downstream Products

• 1255768-07-0 (-)-dimethyl (3aR,8R,8aR,8bS)-1,3-dioxo-2,8-diphenyl-2,3,3a,4,6,8,8a,8b-octahydrocyclopenta[e]isoindole-7,7(1H)-dicarboxylate 
• 1255768-04-7 (+)-dimethyl (2R)-2-phenyl-4-vinylcyclopent-3-ene-1,1-dicarboxylate 
• 1255768-15-0 (+)-dimethyl (3R,3aS)-4,4,5,5-tetracyano-3-phenyl-1,3,3a,4,5,6-hexahydro-2H-indene-2,2-dicarboxylate 
• 1255768-10-5 (+)-4,5-diethyl 2,2-dimethyl (3R,3aS)-3-phenyl-1,3,3a,6-tetrahydro-2H-indene-2,2,4,5-tetracarboxylate 
• 1255768-13-8 (-)-dimethyl (1R,5aR,9aR,9bR)-6,9-dioxo-1-phenyl-1,3,5,5a,6,9,9a,9b-octahydro-2H-cyclopenta[a]naphthalene-2,2-dicarboxylate 
• 1284206-83-2 2,2-dimethyl (3S,3aR)-5-oxo-3-phenyl-1,2,3,3a,4,5-hexahydropentalene-2,2-dicarboxylate 

Relevant academic research and scientific papers

Platinum(II) chloride-catalyzed stereoselective domino enyne isomerization/diels-alder reaction

Chiral 1,6-enynes were prepared via Ir-catalyzed allylic substitutions. Their platinum(II) chloride-catalyzed domino enyne isomerization/Diels-Alder reaction provided stereoselective access to complex heterocycles. Very high diastereoselectivity was induc