One-pot synthesis of high-index faceted AgCl nanocrystals with trapezohedral, concave hexoctahedral structures and their photocatalytic activity

Nanoscale ◽  
2015 ◽  
Vol 7 (27) ◽  
pp. 11591-11601 ◽  
Author(s):  
Haibin Zhang ◽  
Yonggang Lu ◽  
Hong Liu ◽  
Jingzhong Fang
Keyword(s):  
Photocatalytic Activity ◽  
Solvothermal Synthesis ◽  
Semiconductor Nanocrystals ◽  
High Index ◽  
One Pot ◽  
One Pot Synthesis ◽  
The One ◽  
First Time

The one-pot solvothermal synthesis of AgCl semiconductor nanocrystals with high-index faceted trapezohedral and concave hexoctahedral structures is reported for the first time.

scholarly journals One-pot synthesis of an AgBr/ZnO hierarchical structure with enhanced photocatalytic capacity

RSC Advances ◽  
2017 ◽  
Vol 7 (50) ◽  
pp. 31230-31238 ◽  
Author(s):  
Shengnan Liu ◽  
Min Zheng ◽  
Rui Chen ◽  
Zuoshan Wang
Keyword(s):  
Photocatalytic Activity ◽  
Hierarchical Structure ◽  
Hierarchical Structures ◽  
One Pot ◽  
One Pot Synthesis ◽  
First Time

Hydrangea-like AgBr/ZnO photocatalysts with hierarchical structures and improved photocatalytic activity have been synthesized for the first time.

scholarly journals One-pot synthesis of vanadium-containing silica SBA-3 materials and their catalytic activity for propene oxidation

RSC Advances ◽  
2019 ◽  
Vol 9 (9) ◽  
pp. 4671-4681 ◽  
Author(s):  
Ewa Janiszewska ◽  
Agnieszka Held ◽  
Krystyna Nowińska ◽  
Stanisław Kowalak
Keyword(s):  
Catalytic Activity ◽  
One Pot ◽  
Propene Oxidation ◽  
One Pot Synthesis ◽  
The One ◽  
First Time

Efficient SBA-3 vanadosilicate catalysts for propene oxidation obtained for the first time by the one-pot synthesis.

Identifying the existence of highly-fluorescent carboxylic group-rich carbon nanodots during a one-pot synthesis of branched polyethylenimine-passivated amine group-rich carbon nanodots

RSC Advances ◽  
2015 ◽  
Vol 5 (51) ◽  
pp. 40588-40594 ◽  
Author(s):  
Dan-Dan Liu ◽  
Hua Su ◽  
Qian Cao ◽  
Xue-Yi Le ◽  
Zong-Wan Mao
Keyword(s):  
Citric Acid ◽  
Carbon Nanodots ◽  
Amine Group ◽  
Carboxylic Group ◽  
One Pot ◽  
One Pot Synthesis ◽  
Branched Polyethylenimine ◽  
The One ◽  
First Time

The co-existence of carboxylic group-rich C-Dots and amine group-rich C-Dots during the one-pot pyrolysis of citric acid and bPEI was identified for the first time.

Application of Saccharin as an Acidic Partner in the Ugi Reaction for the One-Pot Synthesis of 3-Iminosaccharins

Synlett ◽  
2017 ◽  
Vol 28 (10) ◽  
pp. 1214-1218 ◽  
Author(s):  
Sorour Ramezanpour ◽  
Zahra Bigdeli ◽  
Nahid Alavijeh ◽  
Frank Rominger
Keyword(s):  
Carboxylic Acid ◽  
Ugi Reaction ◽  
One Pot ◽  
Acid Component ◽  
Multicomponent Condensation ◽  
One Pot Synthesis ◽  
The One ◽  
First Time

The use of saccharin as a replacement for the carboxylic acid component in an Ugi multicomponent condensation leading to [(1,1-dioxido-1,2-benzisothiazol-3-yl)amino]acetamide (3-iminosaccharin) derivatives is described for the first time.

scholarly journals One-pot synthesis of meso-alkyl substituted isocorroles: the reaction of a triarylcorrole with Grignard reagent

2010 ◽  
Vol 14 (08) ◽  
pp. 752-757 ◽  
Author(s):  
Sara Nardis ◽  
Giuseppe Pomarico ◽  
Federica Mandoj ◽  
Frank R. Fronczek ◽  
Kevin M. Smith ◽  
...  
Keyword(s):  
Substitution Reaction ◽  
Grignard Reagent ◽  
One Pot ◽  
One Pot Synthesis ◽  
The One ◽  
First Time ◽  
Ddq Oxidation ◽  
The Way

The reaction of 5,10,15-tritolylcorrole with EtMgBr opens the way for novel functionalizations of the corrole ring. DDQ oxidation of the macrocycle, followed by addition of the Grignard reagent, led to the formation of 5- and 10-alkyl substituted isocorroles in satisfying yields. Together with the one-pot formation of these isocorrole isomers, the use of such a nucleophile evidenced the competitive reactivity of the macrocycle β-positions, leading to the formation of 2-bromo- and 3-bromo-5,10,15-tritolylcorrole. While the formation of these monobromocorrole derivatives is not unprecedented, this is the first time the isomers have been separated and fully characterized. Furthermore, the higher yields of the 2-substituted species highlight a useful regioselectivity for the substitution reaction.

An Overview of the One-pot Synthesis of Imidazolines

2020 ◽  
Vol 24 (20) ◽  
pp. 2341-2355
Author(s):  
Thaipparambil Aneeja ◽  
Sankaran Radhika ◽  
Mohan Neetha ◽  
Gopinathan Anilkumar
Keyword(s):  
Asymmetric Catalysis ◽  
Organic Compounds ◽  
Ring Opening ◽  
Ecological Impact ◽  
Chiral Auxiliary ◽  
One Pot ◽  
One Pot Synthesis ◽  
The One ◽  
Synthetic Intermediate ◽  
Heterocyclic Moiety

One-pot syntheses are a simple, efficient and easy methodology, which are widely used for the synthesis of organic compounds. Imidazoline is a valuable heterocyclic moiety used as a synthetic intermediate, chiral auxiliary, chiral catalyst and a ligand for asymmetric catalysis. Imidazole is a fundamental unit of biomolecules that can be easily prepared from imidazolines. The one-pot method is an impressive approach to synthesize organic compounds as it minimizes the reaction time, separation procedures, and ecological impact. Many significant one-pot methods such as N-bromosuccinimide mediated reaction, ring-opening of tetrahydrofuran, triflic anhydrate mediated reaction, etc. were reported for imidazoline synthesis. This review describes an overview of the one-pot synthesis of imidazolines and covers literature up to 2020.

An Expeditious One-Pot Three-Component Synthesis of 4-Aryl-3,4-dihydrobenzo[g] quinoline-2,5,10(1H)-triones under Green Conditions

2020 ◽  
Vol 23 (23) ◽  
pp. 2626-2634
Author(s):  
Saiedeh Kamalifar ◽  
Hamzeh Kiyani
Keyword(s):  
Reaction Medium ◽  
Meldrum's Acid ◽  
Meldrum’S Acid ◽  
One Pot ◽  
One Pot Synthesis ◽  
Substituted Benzaldehydes ◽  
High Yields ◽  
First Time ◽  
Green Conditions

: An efficient and facial one-pot synthesis of 4-aryl-3,4-dihydrobenzo[g]quinoline- 2,5,10(1H)-triones was developed for the first time. The process proceeded via the three-component cyclocondensation of 2-amino-1,4-naphthoquinone with Meldrum’s acid and substituted benzaldehydes under green conditions. The fused 3,4-dihydropyridin-2(1H)- one-ring naphthoquinones have been synthesized with good to high yields in refluxing ethanol as a green reaction medium. This protocol is simple and effective as well as does not involve the assistance of the catalyst, additive, or hazardous solvents.

Pt NPs@GO as a highly efficient and reusable catalyst for one-pot synthesis of acridinedione derivatives

RSC Advances ◽  
2015 ◽  
Vol 5 (61) ◽  
pp. 49295-49300 ◽  
Author(s):  
Handan Pamuk ◽  
Burak Aday ◽  
Fatih Şen ◽  
Muharrem Kaya
Keyword(s):  
Aromatic Aldehydes ◽  
Reusable Catalyst ◽  
One Pot ◽  
Highly Efficient ◽  
One Pot Synthesis ◽  
First Time

Pt NPs@GO has been used for the first time for synthesizing acridinedione from dimedone, aromatic aldehydes and various amines as a catalyst.

Catalyst-Free One-Pot Synthesis of Novel Heteroarylamine Substituted Furo[3,2-c]coumarins

Synlett ◽  
2018 ◽  
Vol 29 (12) ◽  
pp. 1589-1592 ◽  
Author(s):  
Abolfazl Olyaei ◽  
Mahnaz Saraei ◽  
Reyhaneh Khoeiniha
Keyword(s):  
Michael Addition ◽  
Aldol Condensation ◽  
Ring Closure ◽  
Dehydration Reaction ◽  
One Pot ◽  
Catalyst Free ◽  
One Pot Synthesis ◽  
Tandem Process ◽  
First Time

A high-yielding cyclocondensation of 4-hydroxycoumarin, phenylglyoxal monohydrate, and heteroarylamines proceeds without catalysis, which gives novel functionalized furo[3,2-c]coumarins and heteroarylamino alkylation of coumarin products in acetonitrile under reflux, is reported for the first time. This tandem process involves sequentially an aldol condensation, Michael addition, a ring closure, and dehydration reaction.

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