1030-09-7

Upstream product

• 332-77-4 2,5-dihydro-2,5-dimethoxyfuran 
• 112371-43-4 4-methoxy-4-phenylbut-2-enal 
• 88430-52-8 1,4-diphenylbutadiene monoepoxide 
• 50874-13-0 1-methoxy-1-phenylpropyne 
• 54277-08-6 meso-1,4-diphenyl-but-2-yne-1,4-diol 
• 107487-46-7 (RS,SR)-4-methoxy-1,4-diphenylbut-2-yn-1-ol 
• 83564-77-6 4-methoxy-4-phenylbut-2-yn-1-ol 
• 107487-40-1 (E)-4-methoxy-1,4-diphenylbut-2-en-1-one 
• 107487-48-9 (E)-4-methoxy-4-phenylbut-2-ene-1-ol 

Downstream Products

• 17572-77-9 (3E)-1,4-diphenylbut-3-en-1-one 
• 128237-82-1 1,4-dimethoxy-1,4-diphenylbut-2-ene 

Relevant academic research and scientific papers

Synthesis of 2,5-dihydro-2,5-diphenylfuran

2,5-Dihydro-2,5-diphenylfuran (4) has been synthesized by the reaction of phenylmagnesium bromide with 2,5-dibromo-2,5-dihydrofuran (3).Reaction of 2,5-dihydro-2,5-dimethoxyfuran (1) with phenylmagnesium bromide and phenyllithium however leads to ring ope

Nucleophilic Attack on a Carbonyl Group Conjugated to a Chiral Centre: A Search For a Vinylogous Cram's Rule

In a search for a vinylogous version of Cram's rule, 1,4-diphenylbut-2-ene-1,4-dione (5), 4-methoxy-1,4-diphenylbut-2-en-1-one (9), and hex-3-ene-2,5-dione (13) are found to be reduced with low or negligible diastereoselectivity.Similarly, the phenyl Grignard reagent showed no diastereoselectivity in its reaction with 4-methoxy-4-phenylbut-2-enal (12)