502690-27-9

Upstream product

• 502690-32-6 2-[2,2-dimethyl-6-(4-phenyl-butyl)-[1,3]dioxan-4-yl]-N-methoxy-N-methyl-acetamide 
• 1730-25-2 allylmagnesium bromide 
• 502690-38-2 (5R)-5-hydroxy-N-methoxy-N-methyl-3-oxo-9-phenylnonanamide 
• 502690-28-0 (3R,5R)-3,5-Dihydroxy-9-phenyl-nonanoic acid methoxy-methyl-amide 
• 502690-37-1 1-morpholin-4-yl-[(2S,3R)-3-(4-phenyl-butyl)-oxiranyl]-methanone 
• 502690-31-5 (4S,5R)-4,5-epoxy-N-methoxy-N-methyl-3-oxo-9-phenylnonanamide 
• 502690-29-1 (2S,3R)-3-(4-phenyl-butyl)-oxirane-2-carboxylic acid methylamide 
• 502690-30-4 (2S,3R)-3-(4-phenyl-butyl)-oxirane-2-carboxylic acid methyl ester 

Relevant academic research and scientific papers

Catalytic asymmetric synthesis of both syn- and anti-3,5-dihydroxy esters: application to 1,3-polyol/alpha-pyrone natural product synthesis.

[reaction: see text] We describe a catalytic asymmetric synthesis of both syn- and anti-3,5-dihydroxy esters. The method relies upon catalytic asymmetric epoxidation of alpha,beta-unsaturated imidazolides and amides, using lanthanide-BINOL complexes, and