220944-25-2

Upstream product

• 77943-39-6 4-methyl-5-phenyloxazolidin-2-one 
• 110-44-1 sorbic Acid 

Downstream Products

• 500102-39-6 1-[(E)-(1S,2S)-1-((E)-4-Benzyloxy-but-2-enyl)-2-benzyloxymethyl-hexa-3,5-dienyloxymethyl]-4-methoxy-benzene 
• 500102-40-9 2-[(1R,2R,3S,4S)-3-Benzyloxymethyl-4-(4-methoxy-benzyloxy)-2-((Z)-propenyl)-cyclopentylmethyl]-[1,3]dioxolane 
• 500102-36-3 {2-[(4S,5S)-5-((E)-Buta-1,3-dienyl)-2-(4-methoxy-phenyl)-[1,3]dioxan-4-yl]-ethoxy}-triisopropyl-silane 
• 500102-38-5 (E)-4-[(4S,5S)-5-((E)-Buta-1,3-dienyl)-2-(4-methoxy-phenyl)-[1,3]dioxan-4-yl]-but-2-enoic acid methyl ester 
• 500102-37-4 [(4S,5S)-5-((E)-Buta-1,3-dienyl)-2-(4-methoxy-phenyl)-[1,3]dioxan-4-yl]-acetaldehyde 
• 921763-77-1 (4R,5S)-4-methyl-3-((E)-(R)-2-methyl-hexa-3,5-dienoyl)-5-phenyl-oxazolidin-2-one 

Relevant academic research and scientific papers

Regio- and diastereoselective boron-mediated aldol reactions of chiral α,β,γ,δ-unsaturated N-acyloxazolidinones

Chiral N-acyloxazolidinones derived from conjugated dienoic acids undergo boron-mediated aldol condensation in good yield and with high regio- and diastereoselectivity to provide a convenient method for introducing a 1,3-diene subunit. The condensation of