500056-38-2

Upstream product

• 50-00-0 formaldehyd 
• 216690-20-9 4-(4-fluoro-phenyl)-piperidine-3-carboxylic acid ethyl ester 
• 18861-57-9 ethyl (E)-2-cyano-3-(4-fluorophenyl)-2-propenoate 
• 500056-31-5 4-(4-fluoro-phenyl)-3,4,5,6-tetrahydro-pyridine-3-carboxylic acid ethyl ester 
• 500056-27-9 2-aminomethyl-5,5-diethoxy-3-(4-fluoro-phenyl)-pentanoic acid ethyl ester 
• 500056-23-5 2-cyano-5,5-diethoxy-3-(4-fluoro-phenyl)-pentanoic acid ethyl ester 

Relevant academic research and scientific papers

High-pressure promoted cycloadditions of enol ethers and 3-aryl-2-cyano-2-propenoates

The high-pressure promoted cycloadditions of enol ethers (1) and alkyl 3-aryl-2-cyano-2-propenoates (2) lead stereoselectively in high yields to 2,6-dialkoxy-4-aryl-3,4-dihydro-2H- pyran-5-carbonitriles (3). These cycloadducts have a high potential for further synthesis due to the presence of various functionalities. This is illustrated with some representative conversions. As reactive cyclic ketene acetals the cycloadducts 3 were easily hydrolyzed to aldehydes (6) or ketones or alcoholized to acetals having additional ester and cyano groups (5). Removal of the ester group by decarboxylation gave γ-cyano acetals (7), which were further reduced to δ-amino acetals (8). Selective reduction of the cyano group gave access to acetals of β-amino acid esters (9). The potential of such amino acid esters is demonstrated in a straightforward synthesis of a paroxetin precursor 17 from 13. Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002.