Full paper/MémoireCerium(IV) triflate-catalyzed domino annulation approaches to the synthesis of highly substituted piperidines
-
Add time:08/27/2019 Source:sciencedirect.com
A simple, diastereoselective, inexpensive, and efficient route for the synthesis of highly functionalized piperidines by the condensation of β-keto-esters, aromatic aldehydes and anilines using cerium(IV) triflate as a catalyst is described. In most cases, the piperidine precipitates out of the solution.
We also recommend Trading Suppliers and Manufacturers of 4-(3-METHYLPHENYL)PIPERIDINE (cas 111153-83-4). Pls Click Website Link as below: cas 111153-83-4 suppliers
Prev:The nuclear PP1 interacting protein ZAP3 (ZAP) is a putative nucleoside kinase that complexes with SAM68, CIA, NF110 (cas 111150-22-2)/45, and HNRNP-G
Next:Original articleSynthesis and anticancer activities of ceritinib analogs modified in the terminal piperidine ring) - 【Back】【Close 】【Print】【Add to favorite 】
- Related Information
- Synthesis and optimization of novel (3S,5R)-5-(2,2-dimethyl-5-oxo-4-phenylpiperazin-1-yl)piperidine-3-carboxamides as orally active renin inhibitors08/30/2019
- Preparation of 2,3-trans-substituted piperidines from optically active β-amino-α-methylene esters: Synthesis of optically active (2S,3R)-(−)-epi-CP-99,99408/29/2019
- Original articleSynthesis and anticancer activities of ceritinib analogs modified in the terminal piperidine ring08/28/2019
