COA of Formula: C8H7NO3. I found the field of Chemistry very interesting. Saw the article Compartmentalized Nanoreactors for One-Pot Redox-Driven Transformations published in 2019.0, Reprint Addresses Weck, M (corresponding author), NYU, Mol Design Inst, 550 1St Ave, New York, NY 10003 USA.; Weck, M (corresponding author), NYU, Dept Chem, New York, NY 10003 USA.. The CAS is 100-19-6. Through research, I have a further understanding and discovery of 1-(4-Nitrophenyl)ethanone.
This contribution introduces poly(2-oxazoline)-based shell cross-linked micelles (SCMs) as nanoreactors to realize one-pot redox-driven deracemizations of secondary alcohols in aqueous media. TEMPO and Rh-TsDPEN moieties are spatially positioned into the hydrophilic corona and the hydrophobic micelle core, respectively. TEMPO catalyzes the oxidation of racemic secondary alcohols into ketones, while Rh-TsDPEN catalyzes the asymmetric transfer hydrogenation (ATH) of these ketones to afford enantioenriched secondary alcohols. Both catalysts, the Rh-TsDPEN complex and TEMPO, are incompatible with each other and the SCMs are designed to provide indispensable catalyst site isolation. Kinetic studies show that the SCMs enhance the reactivity of the immobilized catalysts, in comparison to those for the unsupported analogues under the same reaction conditions. Our nanoreactors can perform deracemizations on a broad range of secondary alcohol substrates and are reusable in a continuous manner while maintaining high activity.
Welcome to talk about 100-19-6, If you have any questions, you can contact Qu, PY; Kuepfert, M; Jockusch, S; Weck, M or send Email.. COA of Formula: C8H7NO3
Reference:
Benzodioxan,
,1,4-Benzodioxane | C8H8O2 – PubChem