Results 41 to 50 of about 41,666 (217)

Epoxidation of Methyl Esters as Valuable Biomolecules: Monitoring of Reaction

open access: yesMolecules, 2023
The paper is focused on the epoxidation of methyl esters prepared from oil crops with various profiles of higher fatty acids, especially unsaturated, which are mainly contained in the non-edible linseed and Camelina sativa oil (second generation).
Martin Hájek   +4 more
doaj   +1 more source

P450BM3-Catalyzed Oxidations Employing Dual Functional Small Molecules [PDF]

open access: yes, 2019
A set of dual functional small molecules (DFSMs) containing different amino acids has been synthesized and employed together with three different variants of the cytochrome P450 monooxygenase P450BM3 from Bacillus megaterium in H2O2-dependent oxidation
Girhard, Marco   +5 more
core   +1 more source

Catalytic and mechanistic studies into the epoxidation of styrenes using manganese complexes of structurally similar polyamine ligands [PDF]

open access: yes, 2014
The synthesis and catalytic activity of manganese(ii) complexes of two polyamine ligands is reported which highlights how a small structural change in the ligand affects the overall catalytic behaviour.
Al-Safadi, R   +5 more
core   +1 more source

Insights into the function of silver as an oxidation catalyst by ab initio, atomistic thermodynamics [PDF]

open access: yesPhys. Rev. B 68, 165412 (2003), 2003
To help understand the high activity of silver as an oxidation catalyst, e.g., for the oxidation of ethylene to epoxide and the dehydrogenation of methanol to formaldehyde, the interaction and stability of oxygen species at the Ag(111) surface has been studied for a wide range of coverages.
arxiv   +1 more source

Mechanistic investigation on oxygen transfer with the manganese-salen complex [PDF]

open access: yes, 2015
The best-known application of salen complexes is the use of a chiral ligand loaded with manganese to form the Jacobsen complex. This organometallic catalyst is used in the epoxidation of unfunctionalized olefins and can achieve very high selectivities ...
Bogaerts, Thomas   +3 more
core   +2 more sources

A continuous protocol for the epoxidation of olefins, monocyclic terpenes, and Alpha Beta Unsaturated Carbonyl Synthons using eco-friendly Flow Reactor Conditions

open access: yesResults in Engineering, 2022
Herein, we report a simple synthetic protocol for selective epoxidation of olefins, monocyclic terpenes, and chalcones using a continuous semi-batch process in good to excellent yields.
Chidambaram R. Ramaswamy   +7 more
doaj  

The stability of 3 transmembrane and 4 transmembrane human vitamin K epoxide reductase models [PDF]

open access: yes, 2016
3 transmembrane and 4 transmembrane helices models are suggested for the human vitamin K epoxide reductase (VKOR). In this study, we investigate the stability of the human 3 transmembrane/4 transmembrane VKOR models employing a coarse-grained normal mode analysis and molecular dynamics simulation.
arxiv   +1 more source

Why is a noble metal catalytically active? The role of the O-Ag interaction in the function of silver as an oxidation catalyst [PDF]

open access: yesPhys. Rev. Lett. 90, 256102 (2003), 2003
Extensive density-functional theory calculations, and taking into account temperature and pressure, affords a comprehensive picture of the behavior and interaction of oxygen and Ag(111), and provides valuable insight into the function of silver as an oxidation catalyst.
arxiv   +1 more source

Total synthesis of aurofusarin: studies on the atropisomeric stability of bis-naphthoquinones [PDF]

open access: yes, 2018
An efficient annulation involving pyrone addition to a quinone and Dieckmann condensation was developed for rapid assembly of a γ-naphthopyrone monomeric precursor to the bis-naphthoquinone natural product aurofusarin.
Allen   +42 more
core   +1 more source

Epoxides and Soluble Epoxide Hydrolase in Cardiovascular Physiology [PDF]

open access: yesPhysiological Reviews, 2012
Epoxyeicosatrienoic acids (EETs) are arachidonic acid metabolites that importantly contribute to vascular and cardiac physiology. The contribution of EETs to vascular and cardiac function is further influenced by soluble epoxide hydrolase (sEH) that degrades EETs to diols. Vascular actions of EETs include dilation and angiogenesis.
openaire   +3 more sources

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