119613-16-0

Upstream product

• 100-39-0 benzyl bromide 
• 119613-21-7 (4S,5S)-2-<2-(1,2-dihydro-4-methoxybenzocyclobuten-1-yl)-ethyl>-4,5-bis(hydroxymethyl)-2-isopropenyl-1,3-dioxolane 
• 100981-86-0 5-(1,2-dihydro-4-methoxybenzocyclobuten-1-yl)-2-methyl-pent-1-en-3-one 
• 125217-40-5 7-(3,3-Dimethoxy-4-methyl-pent-4-enyl)-3-methoxy-bicyclo[4.2.0]octa-1,3,5-triene 
• 119613-20-6 (4R,5R)-diethyl 2-<2-(1,2-dihydro-4-methoxybenzocyclobuten-1-yl)-ethyl>-2-isopropenyl-1,3-dioxolane-4,5-dicarboxylate 

Relevant academic research and scientific papers

ASYMMETRIC SYNTHESIS OF TRANS-BENZOPERHYDROINDAN: ASYMMETRIC INDUCTION IN INTRAMOLECULAR DIELS-ALDER REACTION OF O-QUINODIMETHANES

Diastereofacial selection has been shown to occur in the asymmetric intramolecular Diels-Alder reactions of chiral o-quinodimethanes generated by thermal ring-opening of the chiral benzocyclobutenes (1a,b,e,f).