132934-10-2

Upstream product

• 132934-06-6 1-(1-hydroxy-2-trimethylsilylmethylprop-2-enyl)-4-methoxy-2-(4-methylthiobut-3-enyl)benzene 
• 132934-19-1 3-(2'-bromo-5'-methoxyphenyl)propan-1-ol 
• 146175-93-1 3-(2'-bromo-5'-methoxyphenyl)propanal 
• 146176-00-3 4-Methoxy-2-((E)-4-methylsulfanyl-but-3-enyl)-benzaldehyde 
• 132934-15-7 1-Bromo-4-methoxy-2-((E)-4-methylsulfanyl-but-3-enyl)-benzene 
• 7252-82-6 3-(3-methoxyphenyl)propan-1-ol 
• 6099-04-3 trans-3-methoxycinnamic acid 
• 146176-01-4 2-((E)-4-Benzyloxy-but-3-enyl)-4-methoxy-benzaldehyde 
• 132934-14-6 2-((E)-4-Benzyloxy-but-3-enyl)-1-bromo-4-methoxy-benzene 
• 132934-04-4 2-(4-benzyloxybut-3-enyl)-1-(1-hydroxy-2-trimethylsilylprop-2-enyl)-4-methoxybenzene 

Relevant academic research and scientific papers

Intramolecular Cycloadditions: Synthesis of 1-Methylene-2,3,3a,4,5,9b-hexahydro-1H-benzindenes and an unsuccessful approach to Ergot Alkaloids

1-(1-Hydroxy-2-trimethylsilylmethylprop-2-enyl)-2-(4-substituted-but-3-enyl)-4-methoxybenzenes, prepared by a short synthesis, underwent intramolecular cycloadditions to produce the title indenes.An analogous intramolecular cycloaddition was attempte

Intramolecular (3+2) Cycloadditions

1-(1-Hydroxy-2-trimethylsilylmethylprop-2-enyl)-2-(4-methoxybut-3-enyl)-4-methoxybenzene, prepared by a short synthesis, underwent (3+2) cycloaddition to form predominantly the cis-fused tricycle 3,7-dimethoxy-1-methylene-2,3,3a,4,5,9b-hexahydro-1H-benze