Name: (S)-2-Ethylpiperidine hydrochlorideOn September 30, 2018 ,《Diastereoselective synthesis of 2-vinylpyrrolidines and 2-vinylpiperidines by the palladium-catalysed cyclization of amino-allylic carbonates containing a chiral protecting group》 was published in ARKIVOC (Gainesville, FL, United States). The article was written by Olszewska, Beata; Jablonska, Aleksandra; Zawisza, Anna. The article contains the following contents:
An efficient diastereoselective synthesis of pyrrolidine- and piperidine-type N-heterocycles was reported, by the intramol. Pd(0)-catalyzed cyclization of amino carbonates containing chiral protecting group. The use of chiral auxiliary in the cyclization gave the corresponding heterocyclic derivatives in excellent yields and with good dr values. In the experiment, the researchers used many compounds, for example, (S)-2-Ethylpiperidine hydrochloride(cas: 558479-16-6Name: (S)-2-Ethylpiperidine hydrochloride)
(S)-2-Ethylpiperidine hydrochloride(cas: 558479-16-6) is a member of piperidine. Piperidine is ubiquitous structural motif widely occurred in diverse synthetically and naturally occurring bioactive molecules. Piperidines are an immensely important class of compounds medicinally: the piperidine ring is the most common heterocyclic subunit among FDA approved drugs.Name: (S)-2-Ethylpiperidine hydrochloride
Referemce:
Piperidine – Wikipedia,
Piperidine | C5H11N – PubChem