Epoxidation - Open Access .click

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Molecular propensity as a driver for explorative reactivity studies

, 2016
Quantum chemical studies of reactivity involve calculations on a large number of molecular structures and comparison of their energies. Already the set-up of these calculations limits the scope of the results that one will obtain, because several system ...
Reiher, Markus, Vaucher, Alain C.
core +2 more sources

Epoxidation of 1,7-octadiene by Pseudomonas oleovorans: fermentation in the presence of cyclohexane [PDF]

, 1977
Robert D. Schwartz, C. J. McCoy
openalex +1 more source

Safranal epoxide – A potential source for diverse therapeutic applications

Saudi Pharmaceutical Journal, 2018
Safranal is an organic compound isolated from saffron oil. Photo epoxidation and thermal reactions of safranal can be a significant tool for the design of drugs to act as anticancer agents and potent chemoprevention.
Suzan Khayyat, Eman Elgendy
doaj

Enhanced Catalytic Performance of Sn Single-Atom Doped CuO with Oxygen Vacancies for Efficient Epoxidation of α-Olefins

Molecules
Epoxidation of long-chain α-olefins (LAOs) is a process of paramount importance, particularly in the preparation of epoxides. Traditional epoxidation methods, such as the chlorohydrin method and peracid method, suffer from issues such as poor selectivity,
Min Zhang +11 more
doaj +1 more source

Enzymatic epoxidation: synthesis of 7,8-epoxy-1-octene, 1,2-7,8-diepoxyoctane, and 1,2-Epoxyoctane by Pseudomonas oleovorans [PDF]

, 1976
Robert D. Schwartz, C. J. McCoy
openalex +1 more source

Pseudomonas oleovorans Hydroxylation-Epoxidation System: Additional Strain Improvements [PDF]