203259-90-9

Upstream product

• 694-05-3 1,2,3,6-tetrahydropyridine 
• 1885-14-9 phenyl chloroformate 

Downstream Products

• 612485-53-7 (rac)-N-phenoxycarbonyl-3,4-epoxypiperidine 
• 203259-94-3 2-cyano-1,4,5,6-tetrahydro-1-pyridinecarboxylic acid phenyl ester 
• 612485-59-3 (+)-(3R,4R)-N-phenoxycarbonyl-3,4-dihydroxypiperidine 
• 37088-07-6 1,4,5-trideoxy-1,5-imino-D-threo-pentitol 
• 164732-66-5 3,4-dihydro-2H-pyridine-1-carboxylic acid phenyl ester 

Relevant academic research and scientific papers

Engineered P450pyr monooxygenase for asymmetric epoxidation of alkenes with unique and high enantioselectivity

A triple mutant of P450pyr monooxygenase (P450pyrTM) catalysed the epoxidation of several para-substituted styrenes as the first enzyme showing high (R)-enantioselectivity and high conversion, demonstrated a broad substrate range, and showed high enantioselectivity for the epoxidation of an unconjugated 1,1-disubstituted alkene, 2-methyl-3-phenyl-1-propene, and a cyclic alkene, N-phenoxycarbonyl-1,2,5,6-tetrahydropyridine, respectively.

Enantioselective Trans Dihydroxylation of Nonactivated C-C Double Bonds of Aliphatic Heterocycles with Sphingomonas sp. HXN-200

The bacterial strain Sphingomonas sp. HXN-200 was used to catalyze the trans dihydroxylation of N-substituted 1,2,5,6-tetrahydropyridines 1 and 3-pyrrolines 4 giving the corresponding 3,4-dihydroxypiperidines 3 and 3,4-dihydroxypyrrolidines 6, respectivel