130543-45-2

Upstream product

• 130543-50-9 2-bromomethylacrylic acid benzyl ester 
• 116087-65-1 (2S,3R,4R)-2,3,4,5-tetrakis(benzyloxy)pentanal 
• 130543-44-1 1,4,5,6,7-pentabenzyloxy-hept-2-ene 
• 130543-41-8 1,7-(bisbenzyloxy)-4-<(N-phenylcarbamoyl)-oxy>-5,6-epoxy-2-ene 
• 130543-42-9 hept-2-ene-1,7-bisbenzyloxy-4,5,6-triol 4,5-carbonate 
• 130543-43-0 hept-2-ene-1,7-bisbenzyloxy-4,5,6-triol 
• 106319-55-5 (E)-(R)-4-Benzyloxy-1-((2R,3S)-3-benzyloxymethyl-oxiranyl)-but-2-en-1-ol 
• 130543-49-6 (2E,5E)-1,7-Bis-benzyloxy-hepta-2,5-dien-4-ol 
• 100-39-0 benzyl bromide 

Downstream Products

• 130543-46-3 (4R,5S,6R,7R)-5,6,7,8-Tetrakis-benzyloxy-4-(tert-butyl-dimethyl-silanyloxy)-2-methylene-octanoic acid benzyl ester 
• 130543-47-4 (4R,5S,6R,7R)-5,6,7,8-Tetrakis-benzyloxy-4-(tert-butyl-dimethyl-silanyloxy)-2-oxo-octanoic acid benzyl ester 

Relevant academic research and scientific papers

The asymmetric epoxidation of divinyl carbinols: Theory and applications

The asymmetric epoxidation of symmetric divinyl carbinols is illustrative of a reaction process that combines an initial asymmetric synthesis with a subsequent kinetic resolution to provide products with extraordinary levels of enantiomeric purity. The application of this process to the asymmetric synthesis of natural products is presented herein.