Literature DB >> 17325787

Chemo-differentiating ABB' multicomponent reactions. Privileged building blocks.

David Tejedor1, Fernando García-Tellado.   

Abstract

Multicomponent reactions (MCRs) designated as ABB' are defined as those reactions that introduce into the final product one molecule of component A and two molecules of component B in a chemo-differentiating manner. This ability to discriminate the incorporation of component B ensures that these processes maintain the advantages of using multicomponent reactions in diversity-oriented molecular construction. Furthermore, they benefit from the fact that only two reagents need to be mixed together. Component B can be therefore considered to be a privileged building block, and the reactions in which it participates, chemo-differentiating multicomponent reactions. Among the reduced set of compounds capable of acting as such building blocks, we discuss the use of ketenes, terminal conjugated alkynoates, enolisable carbonyl compounds, cyclic enol ethers and cyclic enamines.

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Year:  2006        PMID: 17325787     DOI: 10.1039/b608164a

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


  16 in total

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Journal:  Mol Divers       Date:  2018-06-27       Impact factor: 2.943

3.  One-pot synthesis of densely functionalized cyclic β-aminoesters containing four stereocenters, based on a Et3N-promoted pseudo five-component reaction.

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Review 4.  α-Aminoazoles/azines: key reaction partners for multicomponent reactions.

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5.  A convenient four-component one-pot synthesis of 2-amino-1,3,4-thiadiazoles in water.

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6.  6-Amino-3-methyl-4-(3-nitro-phen-yl)-1-phenyl-1H,4H-pyrano[2,3-c]pyrazole-5-carbonitrile.

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Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2011-05-20

7.  Novel biocompatible core/shell Fe3O4@NFC@Co(ii) as a new catalyst in a multicomponent reaction: an efficient and sustainable methodology and novel reusable material for one-pot synthesis of 4H-pyran and pyranopyrazole in aqueous media.

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Journal:  RSC Adv       Date:  2020-10-08       Impact factor: 4.036

8.  Studies on the interaction of isocyanides with imines: reaction scope and mechanistic variations.

Authors:  Ouldouz Ghashghaei; Consiglia Annamaria Manna; Esther Vicente-García; Marc Revés; Rodolfo Lavilla
Journal:  Beilstein J Org Chem       Date:  2014-01-06       Impact factor: 2.883

9.  Features of the behavior of 4-amino-5-carboxamido-1,2,3-triazole in multicomponent heterocyclizations with carbonyl compounds.

Authors:  Eugene S Gladkov; Katerina A Gura; Svetlana M Sirko; Sergey M Desenko; Ulrich Groth; Valentin A Chebanov
Journal:  Beilstein J Org Chem       Date:  2012-11-30       Impact factor: 2.883

10.  Efficient synthesis of dihydropyrimidinones via a three-component Biginelli-type reaction of urea, alkylaldehyde and arylaldehyde.

Authors:  Haijun Qu; Xuejian Li; Fan Mo; Xufeng Lin
Journal:  Beilstein J Org Chem       Date:  2013-12-11       Impact factor: 2.883

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