144536-31-2

Upstream product

• 143878-63-1 (3S,4S)-5-benzyloxy-syn-3,4-dihydroxy-1-pentene 
• 530-62-1 1,1'-carbonyldiimidazole 
• 143878-62-0 (4S,5S)-4-[(benzyloxy)methyl]-2,2-dimethyl-5-vinyl-1,3-dioxolane 
• 81028-12-8 (4S,5R)-4-benzyloxymethyl-2,2-dimethyl-1,3-dioxolane-5-carboxaldehyde 

Downstream Products

• 144536-34-5 (3E,6Z)-(R)-6-Benzenesulfonyl-1-benzyloxy-octa-3,6-dien-2-ol 
• 144536-33-4 (E)-(R)-2-Acetyl-7-benzyloxy-6-hydroxy-hept-4-enoic acid ethyl ester 
• 147219-88-3 {[(2E)-penta-2,4-diene-1-yloxy]methyl}benzene 
• 144536-32-3 2-((E)-(R)-5-Benzyloxy-4-hydroxy-pent-2-enyl)-malonic acid diethyl ester 
• 182206-15-1 (2S,3S)-1-(benzyloxy)-3-(4-methoxyphenoxy)pent-4-en-2-ol 
• 156713-03-0 (2S,3S)-2-Benzyloxymethyl-3-vinyl-oxirane 
• 120132-30-1 (2S,3R)-2-Benzyloxymethyl-3-vinyl-oxirane 
• 143878-63-1 (3S,4S)-5-benzyloxy-syn-3,4-dihydroxy-1-pentene 
• 58931-16-1 (R)-1-benzyloxypent-4-en-2-ol 

Relevant academic research and scientific papers

Highly regio-, (E)-stereo-, and diastereoselective SN2′ addition of organocuprates to chiral allylic cyclic carbonates

Reaction of the cyclic carbonates of acyclic vinyl diols with RCu(CN)Li· BF3, RCu(CN)MgBr·BF3, or RMgBr·CuI (cat) in THF at -78°C proceeded in SN2′ fashion and resulted in the formation of alkylated (E)-allylic alcohols wi