2022
DOI: 10.2139/ssrn.4278681
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Pyridinic-Nitrogen Containing Ordered Mesoporous Carbons as Nad(P)H Mimics for Borrowing Hydrogen Reactions

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Cited by 2 publications
(3 citation statements)
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“…[7d,15a-c] For instance, Ti 4 + and Ti 3 + are highly prevalent when the particle size reduces below 100 nm. Recently, Corma and co-workers [16,17] have demonstrated using an Au/CeO 2 catalyst that the benzyl alcohol undergoes a rapid and reversible binding to the oxide surface to give the alkoxides. Similarly, the benzyl alcohol 1 a would form an alkoxide to generate surface adsorbed species I in the case of TiO 2 (Scheme 5).…”
Section: Catalystsmentioning
confidence: 99%
“…[7d,15a-c] For instance, Ti 4 + and Ti 3 + are highly prevalent when the particle size reduces below 100 nm. Recently, Corma and co-workers [16,17] have demonstrated using an Au/CeO 2 catalyst that the benzyl alcohol undergoes a rapid and reversible binding to the oxide surface to give the alkoxides. Similarly, the benzyl alcohol 1 a would form an alkoxide to generate surface adsorbed species I in the case of TiO 2 (Scheme 5).…”
Section: Catalystsmentioning
confidence: 99%
“…49 Nitrogen-incorporated mesoporous carbons were explored in recent times for their ability to promote BH reactions. 50,51 Recently, gold nanoparticles deposited on TiO 2 were shown to readily catalyze the mono-alkylation of amines with alcohols as well as the direct condensation of nitroarenes with alcohols to form secondary or tertiary amines. 52,53…”
Section: Introductionmentioning
confidence: 99%
“…49 Nitrogenincorporated mesoporous carbons were explored in recent times for their ability to promote BH reactions. 50,51 Recently, gold nanoparticles deposited on TiO 2 were shown to readily catalyze the mono-alkylation of amines with alcohols as well as the direct condensation of nitroarenes with alcohols to form secondary or tertiary amines. 52,53 Herein, we demonstrate that TiO 2 or titanium dioxide, a commonly used commercial catalyst in organic chemistry, is an effective catalyst for the C-C bond formation of ketones with aryl alcohol to produce the corresponding C-alkylated compounds (Scheme 1) in the absence of any external hydrogen source.…”
Section: Introductionmentioning
confidence: 99%