A Facile Diversity-Oriented Multicomponent One-Pot Synthesis of 3-Amino-6,7-dihydrobenzo[c]thiophen-4(5H)-one Derivatives from α-Oxo-N,S-ketene Acetal

2014 ◽  
Vol 51 (S1) ◽  
pp. E358-E363 ◽  
Author(s):  
Swapnil G. Yerande ◽  
Sunil D. More ◽  
Mayur Bhandari ◽  
Kiran M. Newase ◽  
Kareem Khoury ◽  
...  
Keyword(s):  
One Pot ◽  
One Pot Synthesis ◽  
Ketene Acetal

ChemInform Abstract: A Facile Diversity-Oriented Multicomponent One-Pot Synthesis of 3-Amino-6,7-dihydrobenzo[c]thiophen-4(5H)-one Derivatives from α-Oxo-N,S-ketene Acetal.

ChemInform ◽  
2015 ◽  
Vol 46 (9) ◽  
pp. no-no
Author(s):  
Swapnil G. Yerande ◽  
Sunil D. More ◽  
Mayur Bhandari ◽  
Kiran M. Newase ◽  
Kareem Khoury ◽  
...  
Keyword(s):  
One Pot ◽  
One Pot Synthesis ◽  
Ketene Acetal

One-Pot Synthesis and Conformational Analysis of 6-Membered Cyclic Iodonium Salts

2020 ◽  
Author(s):  
Lucien Caspers ◽  
Julian Spils ◽  
Mattis Damrath ◽  
Enno Lork ◽  
Boris Nachtsheim
Keyword(s):  
Conformational Analysis ◽  
Bronsted Acids ◽  
One Pot ◽  
Benzyl Alcohols ◽  
Iodonium Salts ◽  
Efficient Approach ◽  
One Pot Synthesis ◽  
Diaryliodonium Salts

In this article we describe an efficient approach for the synthesis of cyclic diaryliodonium salts. The method is based on benzyl alcohols as starting materials and consists of an Friedel-Crafts-arylation/oxidation sequence. Besides a deep optimization, particluar focusing on the choice and ratios of the utilized Bronsted-acids and oxidants, we explore the substrate scope of this transformation. We also discuss an interesting isomerism of cyclic iodonium salts substituted with aliphatic substituents at the bridge head carbon. <br>

Facile and Convenient Ag/Cd/Cu Nanoparticle Catalysed One-pot Synthesis of Xanthenes

2017 ◽  
Vol 7 (12) ◽  
pp. 1192-1195
Author(s):  
Y. I. Shaikh ◽  
G. M. Nazeruddin ◽  
Khursheed Ahmed
Keyword(s):  
One Pot ◽  
One Pot Synthesis ◽  
Cu Nanoparticle

Microwave-assisted one-pot synthesis of pyrimido［4,5-b］quinolines derivatives

2013 ◽  
Vol 30 (6) ◽  
pp. 636-642
Author(s):  
Xueli Zhang ◽  
Zhilan Lin ◽  
Huiling Hu ◽  
Jiaxin He ◽  
Yuan Gao
Keyword(s):  
One Pot ◽  
Microwave Assisted ◽  
One Pot Synthesis

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.

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