95526-25-3

Upstream product

• 108-98-5 thiophenol 
• 95526-26-4 4-[1-Hydroxy-meth-(E)-ylidene]-2-[2-(4-methoxy-bicyclo[4.2.0]octa-1⁽⁶⁾,2,4-trien-7-yl)-ethyl]-2-vinyl-dihydro-furan-3-one 
• 95539-89-2 4-Methoxy-3-[2-(4-methoxy-bicyclo[4.2.0]octa-1⁽⁶⁾,2,4-trien-7-yl)-ethyl]-hexa-1,4,5-trien-3-ol 
• 88165-29-1 2-<2-(1,2-dihydro-5-methoxybenzocyclobutenyl)ethyl>-2-ethenyl-2,3,4,5-tetrahydrofuran-3-one 
• 95526-21-9 3-(1,2-dihydro-5-methoxybenzocyclobutenyl)propanal ethylene acetal 
• 95526-23-1 5-(1,2-dihydro-5-methoxybenzocyclobutenyl)-3-hydroxypent-1-ene 
• 88183-21-5 5-(1,2-dihydro-5-methoxybenzocyclobutenyl)pent-1-en-3-one 
• 88165-28-0 3-(1,2-dihydro-5-methoxybenzocyclobutenyl)propanal 
• 1199-31-1 1-cyano-5-methoxybenzocyclobutane 

Downstream Products

• 95526-27-5 C₂₄H₂₄O₃S 

Relevant academic research and scientific papers

A New Synthetic Approach to Bruceantin via an Intramolecular Diels-Alder Reaction: Stereoselective Construction of the Pentacyclic Model System

An efficient synthesis of the pentacyclic system (2) as a model for bruceantin (1) is described.The key feature of the synthesis was a stereoselective intramolecular Diels-Alder reaction of the benzocyclobutene derivatives (15) and (16), which were conven