نتایج جستجو برای: quinones pre

تعداد نتایج: 313968  

Journal: :Canadian Journal of Chemistry 1977

Journal: :Green Chemistry 2022

A simple process to cleave C=C bonds with H 2 O converts cinnamic acids benzaldehydes, benzoic or quinones, selectivity depending on the solvent. comparison of green metrics was performed for conversion ferulic acid vanillin.

Journal: :Plant physiology 1964
R U Makower

Freshly cut slices darken as a result of oxidation of endogenous phenols in reactions catalyzed by polyphenol oxidase. Ascorbic acid, thiols, and other reducing substances prevent enzymic darkening (5, 17). Earlier studies showed that ATP substantially decreased browning in plant tissues, apparently via the reduction of quinones (14). ATP itself is not a reducing agent. The reducing compound is...

Journal: :Molecules 2017
Hubert Antolak Joanna Oracz Anna Otlewska Dorota Żyżelewicz Dorota Kręgiel

The aim of the study was to identify and quantitatively assess of carotenoids and isoprenoid quinones biosynthesized by six different strains of acetic acid bacteria, belonging to genus Asaia, that are common beverage-spoiling bacteria in Europe. Bacterial cultures were conducted in a laboratory liquid culture minimal medium with 2% sucrose. Carotenoids and isoprenoid quinones were investigated...

2015
Nan Zhao NAN ZHAO Gary Hastings

Fourier transform infrared difference spectroscopy (FTIR DS) is widely used to study the structural details of electron transfer cofactors in photosynthetic protein complexes. In photosynthetic proteins quinones play an important role, functioning as a cofactor in light-driven electron transfer. In photosystem I (PS I) phylloquinone (PhQ) functions as an intermediary in electron transfer. To in...

Journal: :The Journal of organic chemistry 2002
Aaron Aponick Ryan S Buzdygon Robert J Tomko Aleem N Fazal Ellen L Shughart Danielle M McMaster Michael C Myers William H Pitcock Carl T Wigal

A series of substituted quinones was alkylated with diethylcadmium. Regiochemistry of addition shifted from quinol formation to conjugate addition as a function of the steric and electronic effects of the substituents.

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