Results 101 to 110 of about 43,788 (301)

Repulsion of flies by a volatile chemical, benzaldehyde.

open access: yes, 2013
Method 1: A) Flies begin near benzaldehyde at start. Data are presented for each of the 3 parts of the assay. Mean ± S.E.M. for 3 experiments. B) Control without benzaldehyde. Mean ± S.E.M. for 3 experiments.
Alexei V. Medvedev (322053)   +2 more
core   +1 more source

Modulation of the selectivity in benzaldehyde hydrogenation by N-doped carbon nanotubes

open access: yes, 2012
Modulation of the selectivity in benzaldehyde hydrogenation by N-doped carbon ...
包信和   +4 more
core  

Asymmetric syntheses of benzaldehyde and o-anisaldehyde methyl isopropyl acetals

open access: yes, 1996
Asymmetric syntheses of (+)-(αR)-benzaldehyde and (+)-(αR)-o-anisaldehyde methyl isopropyl acetals in 93 and > 95% ee respectively using methodology based on the stereoselective reactions of enantiopure (ortho-substituted benzaldehyde) chromium ...
Correia, LMARB   +2 more
core   +1 more source

Impact of Intermediate Wheatgrass an Adjunct Ingredient on the Chemical Composition and Development of Aroma Compounds in Sake Brewing

open access: yesCereal Chemistry, EarlyView.
ABSTRACT Background Replacing a portion of polished rice with intermediate wheatgrass (IWG) could diversify raw materials for sake, but its effects on composition and fermentation outcomes are not well characterized. The objective of this study was to quantify how adjunct form (whole vs.
Takehiro Murai   +2 more
wiley   +1 more source

Hydrogen Migration Enhances Proton‐Coupled Electron Transfer in an S‐Scheme Heterojunction for High‐Efficiency Photocatalysis

open access: yesCarbon Energy, EarlyView.
Precisely directed built‐in electric field in an S‐scheme heterojunction synergizes photogenerated charge separation with interfacial proton migration, thus co‐localizing electrons and protons on the NOH surface and boosting proton‐coupled electron transfer kinetics in the rate‐determining hydrogen release step. ABSTRACT The kinetic bottleneck in solar‐
Qinhao Zhao   +9 more
wiley   +1 more source

Synthesis and Characterization of Fe(III) Chitosan Nanoparticle N-Benzaldehyde Schiff Base for Biomedical Application

open access: yes, 2023
The present study produced and characterised chitosan, chitosan nanoparticle, chitosan n – benzaldehyde Schiff base, chitosan nanoparticle n – benzaldehyde Schiff base, Fe(III) chitosan n – benzaldehyde Schiff base and Fe(III) chitosan nanoparticle n ...
Omamoke Enaroseha   +2 more
core   +1 more source

Coupled Photocatalytic Hydrogen Production With Selective Biomass Valorization via Active Sites Construction and Electron Transport Channels Engineering

open access: yesCarbon Energy, EarlyView.
A ternary CdS/1T‐WS2/CNTs heterojunction is in‐situ constructed via hydrothermal method, which is used for photocatalytic biomass reforming (biomass‐derived alcohols, lignin). It exhibits outstanding performance: H2 production rate of 26.17 mmol/g/h for benzyl alcohol (BA), benzaldehyde (BD) generation rate of 8.29 mmol/g/h, 90.06% BD selectivity, 100%
Ermiao Liang   +11 more
wiley   +1 more source

Effect of Ultrasound on the Green Selective Oxidation of Benzyl Alcohol to Benzaldehyde

open access: yesMolecules, 2019
Oxidation of alcohols plays an important role in industrial chemistry. Novel green techniques, such as sonochemistry, could be economically interesting by improving industrial synthesis yield.
Marion L. Chevallier   +4 more
doaj   +1 more source

Aldol Condensation of Diacetybenzene with Benzaldehyde Containing a Hydroxyl Group Catalyzed by p-Toluenesulfonic Acid

open access: yes, 2009
Using p-toluenesulfonic acid (p-TsOH) as a catalyst, three 1,3-bis[3-(substituted phenyl) acryloyl]benzene derivatives 1 similar to 3, three 1,4-bis[3-(substituted phenyl)acryloyl]benzene derivatives 4 similar to 6 and two intermediate compounds 7, 8 ...
Li, Y   +5 more
core  

Shedding Light on Synthetic Autocatalysis: From Conventional Closed‐Shell Chemistries to Overlooked Open‐Shell Occurrences

open access: yesChemistry – A European Journal, EarlyView.
Why add another catalyst when the product itself holds the power to catalyze its own formation? Autocatalysis in synthetic chemistry enhances reaction efficiency and uncovers novel catalytic behavior across both closed‐shell and open‐shell systems, expanding reactivity and enabling innovative design strategies.
Jaspreet Kaur, Joshua P. Barham
wiley   +1 more source

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