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Recent advances in the transesterification of β-keto esters
MC Hennessy, TP O'Sullivan - RSC advances, 2021 - pubs.rsc.org
The ability to selectively transesterify β-keto esters is a useful transformation in organic
synthesis. The increasing interest in transesterification for the synthesis of compounds of …
synthesis. The increasing interest in transesterification for the synthesis of compounds of …
Sunflower and rapeseed oil transesterification to biodiesel over different nanocrystalline MgO catalysts
The catalytic activity for the production of biodiesel with three morphologically different
nanocrystalline MgO materials prepared using simple, green and reproducible methods was …
nanocrystalline MgO materials prepared using simple, green and reproducible methods was …
β‐Ketoesters: An Overview and It's Applications via Transesterification
The transesterification process has attained more significant importance in synthesizing a
variety of commercial and non‐commercial β‐ketoesters using alcohols and variety of …
variety of commercial and non‐commercial β‐ketoesters using alcohols and variety of …
Addition of N− H and O− H bonds of amines and alcohols to electron-deficient olefins catalyzed by monomeric Copper (I) systems: reaction scope, mechanistic details …
Monomeric copper (I) amido, alkoxide, and aryloxide complexes catalyze the addition of N−
H and O− H bonds of amines and alcohols, respectively, to electron-deficient olefins. The …
H and O− H bonds of amines and alcohols, respectively, to electron-deficient olefins. The …
Synthesis, molecular docking, and biological evaluation of 3-oxo-2-tolylhydrazinylidene-4, 4, 4-trifluorobutanoates bearing higher and natural alcohol moieties as new …
GF Makhaeva, NA Elkina, EV Shchegolkov… - Bioorganic …, 2019 - Elsevier
To search for effective and selective inhibitors of carboxylesterase (CES), a series of 3-oxo-2-
tolylhydrazinylidene-4, 4, 4-trifluorobutanoates bearing higher or natural alcohol moieties …
tolylhydrazinylidene-4, 4, 4-trifluorobutanoates bearing higher or natural alcohol moieties …
Nucleophilic acyl substitutions of esters with protic nucleophiles mediated by amphoteric, oxotitanium, and vanadyl species
CT Chen, JH Kuo, CH Ku, SS Weng… - The Journal of Organic …, 2005 - ACS Publications
A diverse array of oxometallic species were examined as catalysts in nucleophilic acyl
substitution (NAS) reactions of methyl (or ethyl) esters with protic nucleophiles. Among them …
substitution (NAS) reactions of methyl (or ethyl) esters with protic nucleophiles. Among them …
Vanadyl (IV) acetate: a mild and efficient heterogeneous catalyst for the tetrahydropyranylation of alcohols, thiols and phenols
A variety of alcohols, thiols and phenols readily add to 3, 4-dihydro 2H-pyran under mild
conditions in the presence of catalytic amount of vanadyl (IV) acetate to afford the …
conditions in the presence of catalytic amount of vanadyl (IV) acetate to afford the …
Polymer-mounted N3P (MeNCH2CH2) 3N: a green, efficient and recyclable catalyst for room-temperature transesterifications and amidations of unactivated esters
VR Chintareddy, HA Ho, AD Sadow, JG Verkade - Tetrahedron letters, 2011 - Elsevier
Merrifield resin-supported N3P (MeNCH2CH2) 3N shows excellent activity in the
transesterification of higher esters such as glyceryl tribenzoate to methyl esters. The catalyst …
transesterification of higher esters such as glyceryl tribenzoate to methyl esters. The catalyst …
Manganese (II) salts as efficient catalysts for chemo selective transesterification of β-keto esters under non-conventional conditions
G Krishnaiah, B Sandeep, D Kondhare, KC Rajanna… - Tetrahedron …, 2013 - Elsevier
Transesterification of β-ketoesters with various alcohols has been studied under
conventional and non-conventional conditions using desktop chemicals such as Mn (II) salts …
conventional and non-conventional conditions using desktop chemicals such as Mn (II) salts …
Mn (III) salen complex: an efficient reusable acylation catalyst
Mn(III) salen complex: an efficient reusable acylation catalyst - ScienceDirect Skip to main
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