122566-01-2

Upstream product

• 92912-33-9 1-hydroxy-1,3-dihydrobenzothiophene-2,2-dioxide 
• 98-85-1 1-Phenylethanol 
• 122505-26-4 1-(1-Phenyl-ethoxy)-1,3-dihydro-benzo[c]thiophene 2,2-dioxide 
• 624-49-7 dimethylfumarate 
• 1445-91-6 (S)-1-phenylethanol 
• 101196-31-0 1-((S)-1-Phenyl-ethoxy)-1,3-dihydro-benzo[c]thiophene 2,2-dioxide 

Relevant academic research and scientific papers

Asymmetric induction in Diels-Alder reactions of α-alkoxyorthoquinodimethanes

It has been shown that dienophiles cycloadd selectively to one face of o-quinodimethanes (o-QDMs) bearing chiral α-alkoxy groups.The face selectivity (diastereoselectivity) increases for the series of chiral groups -OCH(Ph)CH3, -OCH(Ph)CH3(CH3)2, and -OCH

Diastereoselectivity and asymmetric induction in the Diels-Alder reaction of o-quinodimethanes

The extent of asymmetric induction in the bimolecular Diels-Alder reactions of chiral o-quinodimethanes with dimethyl fumarate, methyl acrylate, and maleic anhydride has been studied. o-Quinodimethanes with chiral α-alkoxy groups were prepared from 1-alko