105556-94-3

Upstream product

• 105556-93-2 (3S)-3-methyl-3-p-tolyl-4-pentenol 
• 105556-90-9 (3R)-4,4-ethylenedioxy-3-methyl-3-p-tolylbutan-1-ol 
• 105556-89-6 (3R)-4,4-ethylenedioxy-3-methyl-3-p-tolylbut-1-ene 
• 105556-92-1 (2S)-2-hydroxy-3-methyl-3-p-tolyltetrahydrofuran 
• 155612-31-0 (2R)-2-methyl-2-p-tolyl-3-butenal 
• 367520-82-9 (2S)-2-methyl-2-p-tolylbut-3-en-1-ol 
• 155612-31-0 (S)-2-Methyl-2-p-tolyl-but-3-enal 
• 877077-49-1 (R)-(+)-2-(methoxycarbonyl)-2-(4-methylphenyl)propionic acid 
• 127047-07-8 (R)-(+)-methyl 3-hydroxy-2-methyl-2-(4-methylphenyl)propionate 

Downstream Products

• 147129-23-5 (S)-4-methyl-4-(p-tolyl)hex-5-enal 

Relevant academic research and scientific papers

Asymmetric Construction of Quaternary Carbons from Chiral Malonates : Total Syntheses of (+)-Epilaurene and (-)-Isolaurene

Enantiomerically pure (+)-epilaurene and (-)-isolaurene were obtained from the chiral malonic acid ester (R)-(+)-4, via the 4-methyl-4-p-tolylhex-5-en-1-al (S)-9 prepared by double Wittig reaction under sonication, which underwent subsequent radical induc