Brief introduction of 15862-72-3

Because enzymes can increase reaction rates by enormous factors and tend to be very specific, Product Details of 15862-72-3, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 15862-72-3

Chemistry is the experimental and theoretical study of materials on their properties at both the macroscopic and microscopic levels.In a patent， Product Details of 15862-72-3, Which mentioned a new discovery about 15862-72-3

2-Fluorobenzaldehyde (1) and pipecolic acid (7) react in dimethyl sulfoxide with potassium carbonate to form benzylidene-oxaindolizidines 4. These diastereomers yield with acids uniform salts, so from 4 with hydrogen chloride results (E)-3-(2-fluorobenzylidene)-1-[1,2-bis(2-fluorophenyl)-2-hydroxyethyl]-3,4, 5,6-tetrahydropyridinium chloride (6·Cl), elucidated by X-ray structural analysis. Treatment of 6·Cl with alkali hydroxide regenerates 4. Similarly proline (13), when treated with two equivalents of 1, gives rise to oxapyrrolizidines 14. From 14 in presence of 1 the perchlorate of the benzylidene derivative 15·ClO4 can be obtained which is transformed to benzylideneoxapyrrolizidines 15 by bases.

Because enzymes can increase reaction rates by enormous factors and tend to be very specific, Product Details of 15862-72-3, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 15862-72-3

Reference：
Piperidine – Wikipedia,
Piperidine | C5H9063N – PubChem