914618-53-4

Upstream product

• 914618-55-6 (1S,2S)-1,2-bis-benzyloxy-1-p-methoxyphenylbut-3-ene 
• 1189-71-5 isocyanate de chlorosulfonyle 
• 914618-54-5 (1R,2S)-1,2-bis(benzyloxy)-1-p-methoxyphenylbut-3-ene 
• 123-11-5 4-methoxy-benzaldehyde 
• 865565-60-2 (1R,2S)-1-(p-methoxyphenyl)but-3-ene-1,2-diol 

Downstream Products

• 952143-96-3 benzyl (1R,2S)-2-(benzyloxy)-1-(4-methoxyphenyl)-5-oxoheptadecen-(3E)-enyl carbamate 
• 952143-97-4 benzyl (1R,2S)-2-(benzyloxy)-1-(4-methoxyphenyl)-5-oxoheptadecyl carbamate 
• 952143-98-5 (2S,3S)-2-(benzyloxycarbonylamino)-1-methoxy-1,6-dioxooctadecan-3-yl benzoate 
• 952143-95-2 (2S,3S,6S)-methyl 3-(benzyloxy)-6-dodecylpiperidine-2-carboxylate 
• 914618-62-5 3-benzoyloxy-piperidine-1,2-dicarboxylic acid 1-benzyl ester 
• 933471-53-5 (2R,3S)-3-benzyloxycarbonyl-2-p-methoxyphenylpiperidine 
• 914618-52-3 (2R,3S)-1-benzyloxycarbonyl-(3-benzyloxy-2-p-methoxyphenyl)piperidine 
• 914618-57-8 (2R,3S)-1-benzyloxycarbonyl-(3-benzyloxy-2-p-methoxyphenyl)-1,2,3,6-tetrahydropyridine 
• 914618-58-9 (2R,3S)-1-benzyloxycarbonyl-(3-benzoyloxy-2-hydroxymethyl)piperidine 
• 914618-56-7 (1R,2S)-benzyl N-allyl-N-(2-benzyloxy-1-p-methoxyphenylbut-3-enyl)carbamate 

Relevant academic research and scientific papers

An efficient stereoselective synthesis of (+)-deoxoprosophylline

An efficient stereoselective synthesis of (+)-deoxoprosophylline from readily available p-anisaldehyde is described. Key steps in the synthesis include the stereoselective amination of anti-1,2-dibenzyl ether using chlorosulfonyl isocyanate, intermolecula

Synthesis and conformational analysis of 3-hydroxypipecolic acid analogs via CSI-mediated stereoselective amination

A short and efficient stereoselective synthetic approach toward substituted piperidines, involving (2S,3S)-3-hydroxypipecolic acid 1, (2R,3S)-3-hydroxypipecolic acid 3, and their acid-reduced analogs 2 and 4, has been developed. The requisite anti- and sy

Stereoselective synthesis of D-1-deoxynojirimycin and its stereoisomers

A stereoselective synthesis of D-l-deoxynojirimycin (1), D-1-deoxymannojirimycin (2), and D-1-deoxyallonojirimycin (3) was achieved via the regioselective and diastereoselective amination of anti-l,2-dibenzyl ether using chlorosulfonyl isocyanate (CSI), ring-closing metathesis, diastereoselective dihydroxylation, and the regioselective stereochemical inversion of the resulting diol.

An efficient stereoselective synthesis of (2S,3S)-3-hydroxypipecolic acid using chlorosulfonyl isocyanate

An efficient stereoselective syntheses of (2S,3S)-3-hydroxypipecolic acid and (2R,3S)-2-hydroxymethylpiperidin-3-ol were achieved from p-anisaldehyde via the regioselective and diastereoselective introduction of an N-protected amine group using chlorosulf