ChemInform Abstract: A Mild, One-Pot Stadler-Ziegler Synthesis of Arylsulfides Facilitated by Photoredox Catalysis in Batch and Continuous-Flow.

ChemInform ◽  
2013 ◽  
Vol 44 (50) ◽  
pp. no-no
Author(s):  
Xiao Wang ◽  
Gregory D. Cuny ◽  
Timothy Noel
2017 ◽  
Vol 58 (14) ◽  
pp. 1395-1398 ◽  
Author(s):  
Guolin Wu ◽  
Tingting Lv ◽  
Wenhui Mo ◽  
Xiping Yang ◽  
Yu Gao ◽  
...  

2020 ◽  
pp. 104607
Author(s):  
Zeng-Jie Yang ◽  
Qing-Tian Gong ◽  
Yuan Yu ◽  
Wei-Fan Lu ◽  
Zhe-Ning Wu ◽  
...  

2017 ◽  
Vol 56 (22) ◽  
pp. 6294-6297 ◽  
Author(s):  
Clément Audubert ◽  
Oscar Javier Gamboa Marin ◽  
Hélène Lebel

2014 ◽  
Vol 16 (3) ◽  
pp. 896-899 ◽  
Author(s):  
David Cantillo ◽  
Oscar de Frutos ◽  
Juan A. Rincón ◽  
Carlos Mateos ◽  
C. Oliver Kappe

2021 ◽  
Author(s):  
Christopher Jones ◽  
Laurence J. Kershaw Cook ◽  
David Marquez-Gamez ◽  
Konstantin V. Luzyanin ◽  
Jonathan Steed ◽  
...  

ABSTRACT: Many molecular machines are built from modular components with well-defined motile capabilities, such as axles and wheels. Hinges are particularly useful, as they provide the minimum flexibility needed for a simple and pronounced conformational change. Compounds with multiple stable conformers are common, but molecular hinges almost exclusively operate via dihedral rotations rather than truly hinge-like clamping mechanisms. An ideal molecular hinge would better reproduce the behavior of hinged devices, such as gates and tweezers, while remaining soluble, scalable and synthetically versatile. Herein, we describe two isomeric macrocycles with clamp-like open and closed geometries, which crystallize as separate polymorphs but interconvert freely in solution. An unusual one-pot addition cyclization reaction was used to produce the macrocycles on a multigram scale from inexpensive reagents, without supramolecular templating or high-dilution conditions. Using mechanistic information from NMR kinetic studies and at-line mass spectrometry, we developed a semi-continuous flow synthesis with maximum conversions of 85-93% and over 80% selectivity for a single isomer. The macrocycles feature voids that are sterically protected from guests, including reactive species such as fluoride ions, and could therefore serve as chemically inert hinges for adaptive supramolecular receptors and flexible porous materials.


Química Nova ◽  
2021 ◽  
Author(s):  
Vitor Andrade ◽  
Marcio Mattos

THE TELESCOPIC APPROACH AS A TOOL FOR GREEN CHEMISTRY. One-pot reactions have become a powerful tool for the development of sustainable protocols in organic synthesis. In particular, the telescoping of multi-step reactions, i.e., the execution of sequential reactions without isolating and purifying intermediates, reduces the number of steps while preventing waste generation. Additionally, the processes become more sustainable through time, reagents/solvents, energy and cost savings. Therefore, the aim of this work is to summarize and discuss representative one-pot telescoped strategies involving heterocyclic construction, cross-coupling and continuous-flow reactions.


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