Application of 3433-37-2, Because a catalyst decreases the height of the energy barrier, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.3433-37-2, Name is 2-(Hydroxymethyl)piperidine, molecular formula is C6H13NO. In a article£¬once mentioned of 3433-37-2
beta-Hydroxypiperidinecarboxylates: Additions to the chiral pool from bakers’ yeast reductions of beta-ketopiperidinecarboxylates
Reduction of the piperidine keto esters 16-19 using fermenting bakers’ yeast provides high yields of the corresponding hydroxy esters 20, 26, 32 and 37 respectively, exclusively as the cis-diastereoisomers and with good levels (?80%) of enantiomeric enrichment. The relative stereochemistries of the products were deduced from NMR data while the absolute configurations were determined by degradation to known piperidinemethanol derivatives or, in the case of hydroxy ester 37, by homologation to (R)-3-quinuclidinol 41b.
We¡¯ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 3433-37-2, and how the biochemistry of the body works.Application of 3433-37-2
Reference£º
Piperidine – Wikipedia,
Piperidine | C5H2799N – PubChem