Results 71 to 80 of about 14,777 (274)

Cyclohydrocarbonylation-Based Strategy toward Poly- Substituted Piperidines

open access: yes, 2016
Convenient accesses to enantiomerically pure 2-, 2,3-, 2,6-, 2,3,6-substituted piperidines and 1,4-substituted indolizine are described. At first, indium-mediated aminoallylation and -crotylation of aldehydes with (R)-phenylglycinol or (1R,2S)-1-amino-2 ...
Nicolas Zill (1755679)   +5 more
core   +1 more source

Multiscale Design of Anion Exchange Membrane‐Based Seawater Electrolysis for Sustainable Hydrogen Production

open access: yesAdvanced Energy Materials, EarlyView.
Direct seawater electrolysis using anion exchange membranes is emerging as a promising route for sustainable hydrogen production. This review summarizes multiscale design strategies from seawater chemistry and OER–ClER selectivity to catalysts, membranes, MEAs, cells, stacks, and system integration, providing a roadmap toward selective, durable, and ...
Chiho Kim   +7 more
wiley   +1 more source

Pyrrolo[3,2-c]piperidines

open access: yes, 2020
The heterocyclization reaction of oximes derived from aliphatic ketones with acetylene has been applied to piperidone oximes. Pyrrole[3,2-c]piperidines substituted on the six-membered ring have been prepared in this manner.
Sergeeva N.D.   +6 more
core   +2 more sources

Asymmetric Synthesis of Chiral, Nonracemic Trifluoromethyl-Substituted Piperidines and Decahydroquinolines

open access: yes, 2016
Asymmetric Synthesis of Chiral, Nonracemic Trifluoromethyl-Substituted Piperidines and ...
Matthew J. Wyvratt (2093320)   +4 more
core   +2 more sources

How small changes to methylated piperidinium cations impact the synthesis of zeolite SSZ‐39

open access: yesAIChE Journal, EarlyView.
Abstract Here we report a synthesis study of SSZ‐39 with four different organic structure directing agents (OSDA). The goal was to determine how subtle changes to the OSDA architecture impact crystallization kinetics, material composition, and other properties.
Onyinyechukwu Ukagha, Daniel F. Shantz
wiley   +1 more source

Stereoselective, nitro-Mannich/lactamisation cascades for the direct synthesis of heavily decorated 5-nitropiperidin-2-ones and related heterocycles

open access: yesBeilstein Journal of Organic Chemistry, 2012
A versatile nitro-Mannich/lactamisation cascade for the direct stereoselective synthesis of heavily decorated 5-nitropiperidin-2-ones and related heterocycles has been developed. A highly enantioenriched substituted 5-nitropiperidin-2-one was synthesised
Pavol Jakubec   +4 more
doaj   +1 more source

Experimental study of local anesthetic and antiarrhythmic activities of fluorinated ethynylpiperidine derivatives [PDF]

open access: yesBrazilian Journal of Medical and Biological Research
The chemical structure of piperidine has a unique ability to combine with other molecular fragments. This fact makes it possible to actively use it as an effective basis for the creation of new drug-like substances.
E.M. Satbayeva   +10 more
doaj   +1 more source

Efficacy of different dose of dexmedetomidine combined with remifentanil in colonoscopy: a randomized controlled trial

open access: yesBMC Anesthesiology, 2020
Background Dexmedetomidine has advantages during colonoscopy as it allows the patient to cooperate during the procedure. Few studies examined the dexmedetomidine-remifentanil combination.
Li Jia   +5 more
doaj   +1 more source

Structurally simple synthetic 1, 4-disubstituted piperidines with high selectivity for resistant Plasmodium falciparum

open access: yesBMC Pharmacology and Toxicology, 2018
Background Emergence of resistance to artemisinins and some of their combinations in chemotherapy of clinical malaria has intensified the search for novel safe efficacious antimalarial molecules.
Moses N. Ngemenya   +5 more
doaj   +1 more source

Synthesis of Functionalised Piperidines Through a [3 + 3] Cycloaddition Strategy

open access: yes, 2001
A novel approach to functionalised piperidines is described through a [3 + 3] cycloaddition reaction of aziridines with Pd-trimethylenemethane complexes.
Hedley, Simon J.   +4 more
core   +1 more source

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