Results 1 to 10 of about 44,186 (390)
Catalytic Enantioselective Synthesis of 3-Piperidines from Arylboronic Acids and Pyridine [PDF]
Piperidines are frequently found in natural products and are of importance to the pharmaceutical industry. A generally useful asymmetric route to enantiomerically enriched 3-substituted piperidines remains elusive.
Sourabh Mishra, Stephen P Fletcher
exaly +6 more sources
Synthesis of piperidines and pyridine from furfural over a surface single-atom alloy Ru1CoNP catalyst [PDF]
The sustainable production of value-added N-heterocycles from available biomass allows to reduce the reliance on fossil resources and creates possibilities for economically and ecologically improved synthesis of fine and bulk chemicals.
Haifeng Qi+14 more
doaj +3 more sources
[Co(TPP)]‐Catalyzed Formation of Substituted Piperidines [PDF]
Radical cyclization via cobalt(III)‐carbene radical intermediates is a powerful method for the synthesis of (hetero)cyclic structures. Building on the recently reported synthesis of five‐membered N‐heterocyclic pyrrolidines catalyzed by CoII porphyrins ...
Bas De Bruin, Ching-ping Wong
exaly +4 more sources
Mannich Reactions of Carbohydrate Derivatives with Ketones To Afford Polyoxy-Functionalized Piperidines [PDF]
Mannich reactions of carbohydrate derivatives with ketones that afford polyoxy-functionalized piperidines are reported. Ketone nucleophiles (enamines/enolates) were generated in the presence of the amines used for the formation of the iminium ions of ...
Fujie Tanaka, Lingaiah Maram
core +4 more sources
Über γ‐substituierte Piperidine [PDF]
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Ernst Koenigs, Ludwig Neumann
openalex +4 more sources
Gold(I)–catalyzed enantioselective annulations between allenes and alkene-tethered oxime ethers: A straight entry to highly substituted piperidines and aza-bridged medium-sized carbocycles [PDF]
NOTICE: This is the peer reviewed version of the following article: Marcote, D. C., Varela, I., Fernández-Casado, J., Mascareñas, J.L., López*, F. (2019), Gold(I)–catalyzed enantioselective annulations between allenes and alkene-tethered oxime ethers: A
Cagiao Marcote, David+4 more
core +4 more sources
Secondary piperidines are ideal pharmaceutical building blocks owing to the prevalence of piperidines in commercial drugs. Here, we report an electrochemical method for cyanation of the heterocycle adjacent to nitrogen without requiring protection or ...
Shannon L Goes+2 more
exaly +2 more sources
Recent Progresses in the Catalytic Stereoselective Dearomatization of Pyridines. [PDF]
1,2- and 1,4-dihydropyridines and N-substituted 2-pyridones are very important structural motifs due to their synthetic versatility and vast presence in a variety of alkaloids and bioactive molecules.
Comparini LM, Pineschi M.
europepmc +3 more sources
"PIPERIDINE AS A URIC ACID SOLVENT.' [PDF]
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ArthurP. Luff
openalex +4 more sources
An efficient, modular and straightforward entry to tetrahydropyridines and piperidines is reported. This reaction is based on a formal intramolecular hydroalkylation of readily available, properly substituted ynamides which, upon simple activation under ...
Morgan Lecomte, Gwilherm Evano
exaly +2 more sources