scholarly journals Non-metal boron atoms on CuB12 monolayer as efficient catalytic sites for urea production

2022 ◽  
Author(s):  
Changyan Zhu ◽  
Chaoxia Wen ◽  
Miao Wang ◽  
Min Zhang ◽  
Yun Geng ◽  
...  
Keyword(s):  
Low Cost ◽  
Coupling Reaction ◽  
Promising Alternative ◽  
Mild Conditions ◽  
Catalytic Sites ◽  
Urea Production

Electrocatalytic C-N coupling reaction to convert CO2 and N2 into urea under mild conditions has been proposed to be a promising alternative experimentally, but the development of high-stable, low-cost and...

scholarly journals Photocatalytic three-component asymmetric sulfonylation via direct C(sp3)-H functionalization

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Shi Cao ◽  
Wei Hong ◽  
Ziqi Ye ◽  
Lei Gong
Keyword(s):  
Asymmetric Catalysis ◽  
Organic Synthesis ◽  
Photochemical Reaction ◽  
Low Cost ◽  
Bioactive Molecules ◽  
Atom Economy ◽  
Mild Conditions ◽  
Wide Range ◽  
Unsaturated Carbonyl Compound ◽  
Direct Functionalization

AbstractThe direct and selective C(sp3)-H functionalization of cycloalkanes and alkanes is a highly useful process in organic synthesis owing to the low-cost starting materials, the high step and atom economy. Its application to asymmetric catalysis, however, has been scarcely explored. Herein, we disclose our effort toward this goal by incorporation of dual asymmetric photocatalysis by a chiral nickel catalyst and a commercially available organophotocatalyst with a radical relay strategy through sulfur dioxide insertion. Such design leads to the development of three-component asymmetric sulfonylation involving direct functionalization of cycloalkanes, alkanes, toluene derivatives or ethers. The photochemical reaction of a C(sp3)-H precursor, a SO2 surrogate and a common α,β-unsaturated carbonyl compound proceeds smoothly under mild conditions, delivering a wide range of biologically interesting α-C chiral sulfones with high regio- and enantioselectivity (>50 examples, up to >50:1 rr and 95% ee). This method is applicable to late-stage functionalization of bioactive molecules, and provides an appealing access to enantioenriched compounds starting from the abundant hydrocarbon compounds.

scholarly journals Phosphite-Mediated Reductive Cross-Coupling of Isatins and Nitro­styrenes

Synthesis ◽  
2017 ◽  
Vol 49 (12) ◽  
pp. 2663-2676 ◽  
Author(s):  
Somayeh Motevalli ◽  
Jeffrey Johnson
Keyword(s):  
Coupling Reaction ◽  
Cross Coupling ◽  
Reductive Coupling ◽  
Title Reaction ◽  
Dimethyl Phosphite ◽  
Mild Conditions ◽  
Michael Type Addition

A new reductive coupling reaction between N-alkylisatins, dimethyl phosphite, and nitrostyrenes has been developed. The reaction relies on Pudovik addition, subsequent phosphonate–phosphate rearrangement, and Michael-type addition of a transient carbanion on the indolinone with β-nitrostyrenes. This protocol introduces a convenient and versatile method for the construction of polyfunctionalized tertiary phosphates under mild conditions. Chiral general bases catalyze the title reaction with promising levels of enantioselectivity.

Environment-Friendly Design of Lithium Batteries Starting from Biopolymer-Based Electrolyte

NANO ◽  
2021 ◽  
pp. 2130006
Author(s):  
Jiayuan Shi ◽  
Bin Shi
Keyword(s):  
Lithium Batteries ◽  
Lithium Battery ◽  
Water Solubility ◽  
Low Cost ◽  
Organic Liquid ◽  
Adhesive Property ◽  
Environment Friendly ◽  
Battery Materials ◽  
Mild Conditions ◽  
Film Forming

The nondegradable nature and toxicity of organic liquid electrolytes reveal the design deficiency of lithium batteries in environmental protection. Biopolymers can be extracted from biomass under mild conditions, thus they are usually low cost and renewable. The unique characteristics of biopolymers such as water solubility, film-forming capability and adhesive property are of importance for lithium battery. The studies on the biopolymer materials for lithium batteries have been reviewed in this work. Although a lot of work on the biopolymer-based battery materials has been reported, it is still a challenge in the design of lithium battery with zero pollution and zero waste.

Use of RNA isolated from feces as a promising tool for the early detection of colorectal cancer

2012 ◽  
Vol 27 (2) ◽  
pp. 82-89 ◽  
Author(s):  
Giuliano Bernal
Keyword(s):  
Colorectal Cancer ◽  
Early Detection ◽  
Low Cost ◽  
Occult Blood ◽  
Detection Methods ◽  
Fecal Occult Blood ◽  
Public Health Services ◽  
Promising Alternative ◽  
Altered Expression ◽  
Fecal Occult

Colorectal cancer is one of the most common forms of cancer worldwide. Early detection would allow patients to be treated surgically and halt the progression of the disease; however, the current methods of early detection are invasive (colonoscopy and sigmoidoscopy) or have low sensitivity (fecal occult blood test). The altered expression of genes in stool samples of patients with colorectal cancer can be determined by RT-PCR. This is a noninvasive and highly sensitive technique for colorectal cancer screening. According to information gathered in this review and our own experience, the use of fecal RNA to determine early alterations in gene expression due to malignancy appears to be a promising alternative to the current detection methods and owing to its low cost could be implemented in public health services.

scholarly journals General α-Amino 1,3,4-Oxadiazole Synthesis via Late-Stage Reductive Functionalization of Tertiary Amides and Lactams

2021 ◽  
Author(s):  
Daniel Matheau-Raven ◽  
Darren J. Dixon
Keyword(s):  
Carboxylic Acid ◽  
Late Stage ◽  
Coupling Reaction ◽  
Reductive Activation ◽  
Mild Conditions ◽  
Drug Molecules ◽  
Drug Conjugates ◽  
Iminium Ion ◽  
Tertiary Amides ◽  
Coupling Partner

An iridium-catalyzed reductive three-component coupling reaction for the synthesis of medicinally relevant α-amino 1,3,4-oxadiazoles from abundant tertiary amides or lactams, carboxylic acids, and (N-isocyanimino) triphenylphosphorane, is described. Proceeding under mild conditions using (<1 mol%) Vaska’s complex (IrCl(CO)(PPh<sub>3</sub>)<sub>2</sub>) and tetramethyldisiloxane to access the key reactive iminium ion intermediates, a broad range of structurally complex α-amino 1,3,4-oxadiazole architectures were efficiently accessed from diverse carboxylic acid feedstock coupling partners. Extension to α-amino heterodiazole synthesis was readily achieved by exchanging the carboxylic acid coupling partner for C-, S-, or N-centered Brønsted acids, and provided rapid and modular access to these desirable, yet difficult-to-access, heterocycles. Furthermore, the high chemoselectivity of the catalytic reductive activation step allowed the late-stage functionalization of 10 drug molecules, including the synthesis of novel heterodiazole-fused drug-drug conjugates.<br>

Tuning Ferrous Coordination Structure Enables a Highly Reversible Fe Anode for Long-life All-iron Flow Batteries

2021 ◽  
Author(s):  
Yuxi Song ◽  
Kaiyue Zhang ◽  
Xiangrong Li ◽  
Chuanwei Yan ◽  
Qinghua Liu ◽  
...  
Keyword(s):  
Energy Storage ◽  
Large Scale ◽  
Low Cost ◽  
Flow Battery ◽  
Coordination Structure ◽  
Promising Alternative ◽  
Flow Batteries ◽  
Energy Storage Applications ◽  
Long Life ◽  
Hydrolysis Of

Aqueous all-iron flow battery is a promising alternative for large-scale energy storage applications due to low cost and high safety. However, inferior Fe plating/stripping reversibility and hydrolysis of Fe2+ at...

Immobilization of Eversa Lipases on Hydrophobic Supports for Production of Oleate Esters Solvent-Free

2021 ◽  
Author(s):  
Gloria Fernandez-Lorente ◽  
Daniela Remonatto ◽  
J. Vladimir Oliveira ◽  
J. Manuel Guisan ◽  
Débora Oliveira ◽  
...  
Keyword(s):  
Sunflower Oil ◽  
Low Cost ◽  
Industrial Applications ◽  
Solvent Free ◽  
Molar Ratio ◽  
High Catalytic Activity ◽  
Promising Alternative ◽  
Highly Active ◽  
Immobilized Biocatalyst ◽  
Hydrophobic Supports

Abstract Lipases are an important group of biocatalysts for many industrial applications. Two new commercial low-cost lipases Eversa® Transform and Eversa® Transform 2.0 was immobilized on four different hydrophobic supports: Lewatit-DVB, Purolite-DVB, Sepabeads-C18, and Purolite-C18. The performance of immobilized lipases was investigated in the transesterification of sunflower oil solvent-free in an anhydrous medium. Interesting results were obtained for both lipases and the four supports, but with Sepabeads support the lipases Eversa showed high catalytic activity. However, the more stable and efficient derivative was Eversa® Transform immobilized on Sepabeads C-18. A 98 wt% of ethyl ester of fatty acid (FAEE) was obtained, in 3 hours at 40ºC, ethanol/sunflower oil molar ratio of 3:1 and a 10 wt% of the immobilized biocatalyst. After 6 reaction cycles, the immobilized biocatalyst preserved 70 wt% of activity. Both lipases immobilized in Sepabeads C-18 were highly active and stable in the presence of ethanol. The immobilization of Eversa Transform and Eversa Transform 2.0 in hydrophobic supports described in this study appears to be a promising alternative to the immobilization and application of these news lipases still unexplored.

Nickel-Catalyzed Reductive Monofluoroakylation of Alkyl Tosylate with Bromofluoromethane to Access Primary Alkyl Fluoride

2021 ◽  
Author(s):  
Ru Cui ◽  
Jie Sheng ◽  
Bing-Bing Wu ◽  
Duo-Duo Hu ◽  
Hong-Qian Zheng ◽  
...  
Keyword(s):  
Functional Group ◽  
High Efficiency ◽  
Low Cost ◽  
Raw Material ◽  
Mild Conditions

A nickel-catalysed direct terminal monofluormethlyation between alkyl tosylates and a low-cost, industrial raw material bromofluoromethane has been developed. This transformation has demonstrated high efficiency, mild conditions, and good functional-group compatibility....

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