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Eutectic salt-assisted planetary centrifugal deagglomeration for single-crystalline cathode synthesis | Nature Energy
Eutectic salt-assisted planetary centrifugal deagglomeration for single-crystalline cathode synthesis | Nature Energy
Single-crystalline layered oxides are much sought after as they offer high-performance promises in batteries. Here the authors report a facile and scalable planetary centrifugal mixing technique—aided by eutectic lithium salts—that enables the growth of high-quality single-crystalline cathode materials.
Eutectic salt-assisted planetary centrifugal deagglomeration for single-crystalline cathode synthesis | Nature Energy
Proton Shuttle Mechanism for the Oxidation of Formaldehyde by Aldehyde Oxidase: An Electronic Structure Description of Formal Hydride Transfer and “Inhibited” Species | Request PDF
Proton Shuttle Mechanism for the Oxidation of Formaldehyde by Aldehyde Oxidase: An Electronic Structure Description of Formal Hydride Transfer and “Inhibited” Species | Request PDF
Request PDF | On Jan 25, 2019, Tadege Belay and others published Proton Shuttle Mechanism for the Oxidation of Formaldehyde by Aldehyde Oxidase: An Electronic Structure Description of Formal Hydride Transfer and “Inhibited” Species | Find, read and cite all the research you need on ResearchGate
Proton Shuttle Mechanism for the Oxidation of Formaldehyde by Aldehyde Oxidase: An Electronic Structure Description of Formal Hydride Transfer and “Inhibited” Species | Request PDF
Reduction of trans-Cinnamaldehyde - Odinity
Reduction of trans-Cinnamaldehyde - Odinity
By: Jane Huang, Stephanie Thomas and Vasthi Yanes   Chemical Reaction Equation   Reaction Table Introduction The purpose of this lab is to perform a reduction of trans-cinnamaldehyde. This process consists of 1) mixing trans-cinnamaldehyde with sodium borohydride and methanol, 2) employing rota-vap and the rinsing and removal of aqueous layers to purify mixture, 3) drying the precipitate via gravity filtration. The use of metal hydrides, such as sodium borohydride and lithium aluminum hydride, is the most commonly used out of …
Reduction of trans-Cinnamaldehyde - Odinity
The biosynthesis of the cannabinoids | Journal of Cannabis Research | Full Text
The biosynthesis of the cannabinoids | Journal of Cannabis Research | Full Text
Abstract Cannabis has been integral to Eurasian civilization for millennia, but a century of prohibition has limited investigation. With spreading legalization, science is pivoting to study the pharmacopeia of the cannabinoids, and a thorough understanding of their biosynthesis is required to engineer strains with specific cannabinoid profiles. This review surveys the biosynthesis and biochemistry of cannabinoids. The pathways and the enzymes’ mechanisms of action are discussed as is the non-enzymatic decarboxylation of the cannabinoic acids. There are still many gaps in our knowledge about the biosynthesis of the cannabinoids, especially for the minor components, and this review highlights the tools and approaches that will be applied to generate an improved understanding and consequent access to these potentially biomedically-relevant materials. Graphical abstract
The biosynthesis of the cannabinoids | Journal of Cannabis Research | Full Text
Diastereoselective Synthesis of α-C-Arabinofuranosyl Glycine | Request PDF
Diastereoselective Synthesis of α-C-Arabinofuranosyl Glycine | Request PDF
Request PDF | Diastereoselective Synthesis of α-C-Arabinofuranosyl Glycine | Exploiting N-(tert-butoxycarbonyl)-2-(tert-butyldimethylsiloxy)pyrrole (TBSOP) as a masked glycine anion equivalent, a short enantiospecific... | Find, read and cite all the research you need on ResearchGate
Diastereoselective Synthesis of α-C-Arabinofuranosyl Glycine | Request PDF
General Approach to Hydroxylated ?-Amino Acids Exploiting N-( tert-Butoxycarbonyl)-2-(tert-butyldimethylsiloxy)pyrrole | Request PDF
General Approach to Hydroxylated ?-Amino Acids Exploiting N-( tert-Butoxycarbonyl)-2-(tert-butyldimethylsiloxy)pyrrole | Request PDF
Request PDF | General Approach to Hydroxylated ?-Amino Acids Exploiting N-( tert-Butoxycarbonyl)-2-(tert-butyldimethylsiloxy)pyrrole | Racemic β-hydroxy-α-amino acids 7a, 7b and 10 of either threo or erythro configuration have been efficiently synthesized from simple aldehydes,... | Find, read and cite all the research you need on ResearchGate
General Approach to Hydroxylated ?-Amino Acids Exploiting N-( tert-Butoxycarbonyl)-2-(tert-butyldimethylsiloxy)pyrrole | Request PDF