120569-63-3

Downstream Products

• 1037048-29-5 2-benzyl-2-methylbut-3-en-1-ol 
• 1037048-42-2 2-benzyl-2 methyl-1-(4-nitrophenyl)but-3-en-1-ol 
• 1206588-21-7 (4-(2-methyl-1-phenylbut-3-en-2-yloxy)butyl)benzene 
• 1643833-62-8 1-(2-methyl-1-phenylbut-3-en-2-yl)-1H-benzo[d][1,2,3]triazole 
• 1643833-56-0 2-(2-methyl-1-phenylbut-3-en-2-yl)-2H-benzo[d][1,2,3]triazole 
• 37580-42-0 1-phenyl-3-methylbutadiene 
• 1533453-30-3 (E)-5-benzyl-5-methyl-1-phenylhepta-1,6-dien-3-one 
• 1533453-29-0 4-benzyl-1-chloro-4-methylhex-5-en-2-one 
• 1533453-28-9 5-benzyl-2,2,5-trimethylhept-6-en-3-one 
• 1533453-27-8 5-benzyl-2,5-dimethylhept-6-en-3-one 
• 1533453-26-7 6-benzyl-6-methyloct-7-en-4-one 
• 1533453-25-6 4-benzyl-4-methylhex-5-en-2-one 
• 1533453-24-5 3-benzyl-1-(3-bromophenyl)-3-methylpent-4-en-1-one 
• 1533453-23-4 3-benzyl-3-methyl-1-(thiophen-2-yl)pent-4-en-1-one 

Relevant academic research and scientific papers

Ruthenium catalyzed C-C bond formation via transfer hydrogenation: Branch-selective reductive coupling of allenes to paraformaldehyde and higher aldehydes

(Chemical Equation Presented) Under the conditions of ruthenium-catalyzed transfer hydrogenation employing 2-propanol as the terminal reductant, 1,1-disubstituted allenes 1a-h engage in reductive coupling to paraformaldehyde to furnish homoallylic alcohol