「epoxidation」の共起表現一覧(1語右で並び替え)
該当件数 : 22件
sopropoxide is a component of the Sharpless | epoxidation, a method for the synthesis of chiral epoxi |
MDO is considered the reagent of choice for | epoxidation, and in nearly all circumstances is as good |
In the Sharpless | epoxidation, diethyl tartrate and titanium isopropoxide |
The Jacobsen | epoxidation gains its stereoselectivity from a C2 symme |
In addition, a reaction analogous to | epoxidation has been reported involving the metal-catal |
The Shi | epoxidation is a chemical reaction described as an asym |
The | epoxidation mechanism is concerted: the cis or trans ge |
ones to esters (Baeyer-Villiger oxidation), | epoxidation of alkenes (Prilezhaev reaction), oxidation |
droxylation and N-dealkylation, and also by | epoxidation of the naphthalene ring, similar to the met |
sters can also be obtained via nucleophilic | epoxidation of an α,β-unsaturated ester, but that appro |
Jacobsen | epoxidation of alkenes using manganese-salen complex an |
Glycidol is prepared by the | epoxidation of allyl alcohol. |
Sharpless | epoxidation of allyl alcohols using titanium isopropoxi |
Shi | epoxidation of alkenes using oxone and a fructose-deriv |
These compounds are formed by | epoxidation of any one of four double bonds of the arac |
Epoxidation of polycyclic aromatic hydrocarbons can pro | |
Using a base mediated | epoxidation reaction, structure 3 was achieved, which l |
ide at the same time; the carboxylation and | epoxidation reactions are said to be coupled reactions. |
The Jacobsen | Epoxidation, sometimes also referred to as Jacobsen-Kat |
Its main application is in Sharpless | epoxidation, where it serves as a chiral ligand to tita |
tially at the disubstituted alkene, whereas | epoxidation with MCPBA occurs at the trisubstituted alk |
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