2020
DOI: 10.1007/s11030-020-10128-9
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Recent strategies in the synthesis of thiophene derivatives: highlights from the 2012–2020 literature

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Cited by 30 publications
(14 citation statements)
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“…The authors point out that the performance achievement was due to the efficient insertion of CO 2 into the Re(I)–O bond in fac‐[Re(dmb)(CO) 3 {OC 2 H 4 N(C2H 4 OH) 2 }] [170] . Thiophene and polythiophene have brought on much attention due to their high stability and good electron‐conducting properties for the last three decades [171–174] . Also, 3’‐substituted terthiophene shows less steric hindrance and higher conductivity [175] .…”
Section: Electrochemical Co2 Reduction Reaction (Co2rr) Rhenium Bipyridine‐based Catalystsmentioning
confidence: 99%
“…The authors point out that the performance achievement was due to the efficient insertion of CO 2 into the Re(I)–O bond in fac‐[Re(dmb)(CO) 3 {OC 2 H 4 N(C2H 4 OH) 2 }] [170] . Thiophene and polythiophene have brought on much attention due to their high stability and good electron‐conducting properties for the last three decades [171–174] . Also, 3’‐substituted terthiophene shows less steric hindrance and higher conductivity [175] .…”
Section: Electrochemical Co2 Reduction Reaction (Co2rr) Rhenium Bipyridine‐based Catalystsmentioning
confidence: 99%
“…In our previous review, 96 natural thiophene derivatives were listed from various plant species belonging to the Asteraceae family till 2015, with a particular focus on their biosynthesis, bioactivities, and physical and spectral data [8]. Recently, several reviews dealing with synthetic thiophene-based derivatives, including their anti-inflammation and anticancer potentials, spectroscopic properties, and synthesis, were published [21][22][23][24]. On the other side, there is no available review on naturally occurring thiophene derivatives from plant sources.…”
Section: Introductionmentioning
confidence: 99%
“…In this field, thiophene which is a planar five-membered ring heterocyclic cycle has been extensively studied in Organic Electronics due to its facile electropolymerization, its low oxidation potential and its facile chemical modification. [209][210][211][212][213] If thiophene can be electrochemically polymerized, photochemical polymerization reactions have also been developed using potassium dichromate as the oxidant, [214] carbon tetrachloride as the electron acceptor, [215] and even in the presence of iodonium salts. [216][217][218][219] Parallel to this, thiophene was not only used as a monomer for electron or photochemical polymerization but also as a building block for the design of photoinitiators of polymerization.…”
Section: Introductionmentioning
confidence: 99%