Electric Literature of 134441-93-3, 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.134441-93-3, Name is (S)-1-Boc-2-(Hydroxymethyl)piperidine, molecular formula is C11H21NO3. In a article£¬once mentioned of 134441-93-3
A short enantioselective total synthesis of (R)- and (S)-pipecolic acid
A convenient and practical total synthesis of (R)- and (S)-pipecolic acid has been achieved by utilizing chiral cis-aziridine-2-carboxylate as the common synthetic precursor. The synthesis involves regioselective reductive cleavage of the aziridine ring and Wittig olefination as key reactions.
We¡¯ll also look at important developments in the pharmaceutical industry because understanding organic chemistry is important in understanding health, medicine, the role of 134441-93-3, and how the biochemistry of the body works.Electric Literature of 134441-93-3
Reference£º
Piperidine – Wikipedia,
Piperidine | C5H17490N – PubChem