130749-50-7

Upstream product

• 154807-80-4 5-(4-Methoxyphenyl)-2-methyl-2(E)-penten-1-ol 
• 20401-88-1 3-(4-methoxyphenyl)propional 
• 1222923-32-1 (E)-tert-butyl((6-(4-methoxyphenyl)-3-methylhex-3-en-1-yl)oxy)dimethylsilane 
• 122410-12-2 1-Methoxy-4-(4-methyl-3-phenylsulfanylmethoxy-pent-4-enyl)-benzene 

Downstream Products

• 1222923-65-0 (E)-1-(6-(4-methoxyphenyl)-3-methylhex-3-en-1-yl)pyrrolidine-2,5-dione 

Relevant academic research and scientific papers

Enantioselective thiourea-catalyzed cationic polycyclizations

A new thiourea catalyst is reported for the enantioselective cationic polycyclization of hydroxylactams. Both the yield and enantioselectivity of this transformation were found to vary strongly with the identity of a single aromatic residue on a common ca

Does the Wittig-Still rearrangement proceed via a metal free carbanion?

The steric course of [2,3] rearrangements of allyloxy methanides is almost not affected by the counterion (M = Li, Na, K, Rb, Cs) as demonstrated by the nearly metal independent E,Z and anti,syn selectivities of rearrangements 4→6 and 7→8, respectively.