Literature DB >> 26898222

Multicomponent syntheses of functional chromophores.

Lucilla Levi1, Thomas J J Müller.   

Abstract

Multicomponent reactions are a valuable tool for the synthesis of functional π-electron systems. Two different approaches can be taken into account for accessing the target structures. In the more conventional scaffold approach an already existing chromophore is coupled with other components to give a complex functional π-system. Here, electronically monotonous components can also be introduced, which may exert synergistic electronic effects within the novel compound. The more demanding chromophore concept generates a complete π-electron system and a scaffold concurrently. The latter approach is particularly stimulating for methodologists since π-systems might be accessible from simple starting materials. This review encompasses the advances in the preparation of functional π-electron systems via multicomponent processes during the past few years, based both on the scaffold and chromophore concepts. Besides the synthetic strategies the most important properties, i.e. redox potentials, absorption and emission maxima or fluorescence quantum yields, of the synthesized molecules are highlighted.

Year:  2016        PMID: 26898222     DOI: 10.1039/c5cs00805k

Source DB:  PubMed          Journal:  Chem Soc Rev        ISSN: 0306-0012            Impact factor:   54.564


  28 in total

1.  Regioselective synthesis of pyrimidine-fused tetrahydropyridines and pyridines by microwave-assisted one-pot reaction.

Authors:  Pooja Kumari; Rahul Yadav; Ruchi Bharti; Tasneem Parvin
Journal:  Mol Divers       Date:  2019-03-07       Impact factor: 2.943

2.  Design, synthesis and fluorescence property evaluation of blue emitting triazole-linked chromene peptidomimetics.

Authors:  T Jency Mohan; D Bahulayan
Journal:  Mol Divers       Date:  2017-05-06       Impact factor: 2.943

Review 3.  Recent advances in the green synthesis of Betti bases and their applications: a review.

Authors:  Ramsha Iftikhar; Muhammad Kamran; Aleesha Iftikhar; Sadia Parveen; Naila Naeem; Nazia Jamil
Journal:  Mol Divers       Date:  2022-04-21       Impact factor: 2.943

Review 4.  Nanostructured silicate catalysts for environmentally benign Strecker-type reactions: status quo and quo vadis.

Authors:  Vladimir V Kouznetsov; José G Hernández
Journal:  RSC Adv       Date:  2022-07-20       Impact factor: 4.036

5.  One-pot synthesis of naphtho[1,2-e][1,3]oxazines in the presence of FNAOSiPAMP*/CuII as an almond shell based nanocatalyst.

Authors:  Mina Keihanfar; Bi Bi Fatemeh Mirjalili
Journal:  Sci Rep       Date:  2022-10-21       Impact factor: 4.996

6.  One-pot syntheses of blue-luminescent 4-aryl-1H-benzo[f]isoindole-1,3(2H)-diones by T3P® activation of 3-arylpropiolic acids.

Authors:  Melanie Denißen; Alexander Kraus; Guido J Reiss; Thomas J J Müller
Journal:  Beilstein J Org Chem       Date:  2017-11-03       Impact factor: 2.883

Review 7.  Modern Synthetic Avenues for the Preparation of Functional Fluorophores.

Authors:  Fabio de Moliner; Nicola Kielland; Rodolfo Lavilla; Marc Vendrell
Journal:  Angew Chem Int Ed Engl       Date:  2017-02-17       Impact factor: 15.336

8.  A palladium-catalyzed synthesis of (hetero)aryl-substituted imidazoles from aryl halides, imines and carbon monoxide.

Authors:  Jevgenijs Tjutrins; Bruce A Arndtsen
Journal:  Chem Sci       Date:  2016-11-03       Impact factor: 9.825

9.  Bran-New Four-Molecule and Five-Molecule Cascade Reactions for One-Pot Synthesis of Pyrano[3,2-c]chromen-5-ones and Spiro[benzo[b][1,4]diazepine-2,2'-pyrano[3,2-c]chromen]-5'-ones under Catalyst- and Solvent-Free Conditions.

Authors:  Guoxun Zhu; Zhou Yi; Jie Zhou; Zhiyong Chen; Pengran Guo; Yanying Huang; Jianghan Chen; Huacan Song; Wei Yi
Journal:  ACS Omega       Date:  2018-10-18

10.  Thiophene-forming one-pot synthesis of three thienyl-bridged oligophenothiazines and their electronic properties.

Authors:  Dominik Urselmann; Konstantin Deilhof; Bernhard Mayer; Thomas J J Müller
Journal:  Beilstein J Org Chem       Date:  2016-09-20       Impact factor: 2.883

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