695176-84-2

Upstream product

• 485809-19-6 5-phenyl-2-pentenoic acid chloride 
• 695177-15-2 4-[(2E,5R,7S)-1-oxo-9-phenyl-5,7-bis(triethylsilyloxy)-2-nonenyl]morpholine 
• 695177-13-0 ethyl (3S,5S)-7-phenyl-3,5-bis(triethylsilyloxy)heptanoate 
• 695176-65-9 (3S,5S)-7-Phenyl-3,5-bis-triethylsilanyloxy-heptanal 
• 677729-72-5 4-[(2R,3S,5R,7S)-2,3-epoxy-5,7-isopropylidenedioxy-1-oxo-9-phenylnonyl]morpholine 
• 677729-71-4 4-[(2E,5R,7S)-5,7-isopropylidenedioxy-1-oxo-9-phenyl-2-nonenyl]morpholine 
• 502690-43-9 ethyl (3S,5S)-3,5-isopropylidenedioxy-7-phenylheptanoate 
• 677729-70-3 4-[(2R,3S)-2,3-epoxy-1-oxo-5-phenylpentenyl]morpholine 
• 677729-68-9 (E)-1-morpholin-4-yl-5-phenyl-pent-2-en-1-one 
• 502690-42-8 ethyl (3R,5S)-3,5-isopropylidenedioxy-7-phenylheptanoate 
• 502690-22-4 ethyl (3S,5S)-3,5-dihydroxy-7-phenylheptanoate 
• 502690-25-7 ethyl (5S)-5-hydroxy-3-oxo-7-phenylheptanoate 
• 502690-24-6 ethyl (4R,5S)-4,5-epoxy-3-oxo-5-phenethylpentanoate 
• 24271-22-5 5-phenyl-2(E)-pentenoic acid 

Relevant academic research and scientific papers

Strategy for Enantio- and Diastereoselective Syntheses of All Possible Stereoisomers of 1,3-Polyol Arrays Based on a Highly Catalyst-Controlled Epoxidation of α,β-Unsaturated Morpholinyl Amides: Application to Natural Product Synthesis

We describe a new strategy for enantio- and diastereoselective syntheses of all possible stereoisomers of 1,3-polyol arrays. This strategy relies on a highly catalyst-controlled epoxidation of α,β-unsaturated morpholinyl amides promoted by the Sm-BINOL-Ph