152330-77-3

Upstream product

• 1194630-67-5 (R)-4-benzyl-3-{(2R,3S)-3-hydroxy-5-[(4-methoxybenzyl)oxy]-2-methyl-pentanoyl}oxazolidin-2-one 
• 6638-79-5 N,O-dimethylhydroxylamine*hydrochloride 
• 128461-65-4 3-(p-methoxybenzyloxy)propanal 

Downstream Products

• 129985-92-8 <2R,3S>-N-methoxy-N,2-dimethyl-5-<(4-methoxyphenyl)methoxy>-3-<(triethylsilyl)oxy>pentanamide 
• 152330-78-4 (2R,3S)-3-(tert-Butyl-dimethyl-silanyloxy)-5-(4-methoxy-benzyloxy)-2-methyl-pentanoic acid methoxy-methyl-amide 
• 201993-96-6 (2R,3S)-3-Benzyloxymethoxy-5-(4-methoxy-benzyloxy)-2-methyl-pentanoic acid methoxy-methyl-amide 
• 100905-89-3 pamamycin-607 
• 374752-76-8 (2R,3S)-3-Benzyloxymethoxy-5-(4-methoxy-benzyloxy)-2-methyl-pentanal 
• 482626-35-7 (2R,3S,4S,5S)-5-Benzyloxymethoxy-7-(4-methoxy-benzyloxy)-2,4-dimethyl-heptane-1,3-diol 
• 482626-54-0 (R)-2-[(2R,5S)-5-((1R,2S,3R,4R)-2-Benzyloxy-4,6-dihydroxy-1,3-dimethyl-hexyl)-tetrahydro-furan-2-yl]-propionic acid methyl ester 
• 374752-81-5 (2S,3R,4R,5S)-3-Benzyloxy-5-benzyloxymethoxy-7-(4-methoxy-benzyloxy)-2,4-dimethyl-heptanal 
• 482626-37-9 (2R,3S,4R,5S)-3-Benzyloxy-5-benzyloxymethoxy-7-(4-methoxy-benzyloxy)-2,4-dimethyl-heptan-1-ol 
• 482626-36-8 (2R,3S,4S,5S)-5-Benzyloxymethoxy-1-(tert-butyl-dimethyl-silanyloxy)-7-(4-methoxy-benzyloxy)-2,4-dimethyl-heptan-3-ol 
• 374752-94-0 (R)-2-((2R,5S)-5-{(1R,2S,3R)-2-Benzyloxy-1-methyl-3-[(2R,5S)-5-(2-oxo-pentyl)-tetrahydro-furan-2-yl]-butyl}-tetrahydro-furan-2-yl)-propionic acid methyl ester 
• 374752-93-9 (R)-2-{(2R,5S)-5-[(1R,2R,3R,4R)-2-Benzyloxy-6-iodo-1,3-dimethyl-4-((E)-3-oxo-hex-1-enyloxy)-hexyl]-tetrahydro-furan-2-yl}-propionic acid methyl ester 
• 374752-83-7 (4R,5R,6S,7R,8S)-6-Benzyloxy-8-benzyloxymethoxy-10-(4-methoxy-benzyloxy)-5,7-dimethyl-dec-1-en-4-ol 
• 374752-92-8 (R)-2-{(2R,5S)-5-[(1R,2S,3R,4R)-2-Benzyloxy-4-hydroxy-1,3-dimethyl-6-(toluene-4-sulfonyloxy)-hexyl]-tetrahydro-furan-2-yl}-propionic acid methyl ester 

Relevant academic research and scientific papers

Addition of kinetic boron enolates generated from β-alkoxy methyl ketones to aldehydes. Density functional theory calculations on the transition structures

Herein we report that good to excellent levels of 1,5-anti stereoinduction are obtained in boron enolate aldol reactions of 1,2-syn β-alkoxy methyl ketones with achiral aldehydes, when the β-alkoxy protecting group is part of a benzylidene acetal. We have