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Open AccessJournal ArticleDOI

Diversity Oriented Syntheses of Conventional Heterocycles by Smart Multi Component Reactions (MCRs) of the Last Decade

Heiner Eckert
- 20 Jan 2012 - 
- Vol. 17, Iss: 1, pp 1074-1102
TLDR
A collection of smart multicomponent reactions (MCRs) with continuative post condensation cyclizations (PCCs) is presented to construct conventional three- to seven-membered heterocyclic compounds in diversity oriented syntheses (DOS).
Abstract
A collection of smart multicomponent reactions (MCRs) with continuative post condensation cyclizations (PCCs) is presented to construct conventional three- to seven-membered heterocyclic compounds in diversity oriented syntheses (DOS). These will provide a high degree of applying economical and ecological advantages as well as of practicability. Water, ionic liquids, and solvent-less syntheses as well as use of various forms of energy as microwave and ultrasonic irradiation are examined and discussed.

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Recent advances in the synthesis of pyrroles by multicomponent reactions

TL;DR: This work describes the progress made in this area in the period between mid-2009 and the end of 2013 by describing the ready availability of suitably substituted and functionalized pyrrole derivatives.
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Multicomponent reactions in unconventional solvents: state of the art

TL;DR: In this paper, a review summarizes recent results of multicomponent reactions obtained in unconventional media including water, ionic liquids, polyethylene glycol and bio-based solvents.
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Unravelling the labyrinth of palladium-catalysed reactions involving isocyanides

TL;DR: This tutorial review focuses on Isocyanides various applications in chemical synthesis, and the wide range of systems that can be efficiently prepared using this strategy are documented.
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Multicomponent mechanochemical synthesis

TL;DR: Multicomponent reactions promoted by mechanical energy are critically reviewed and new ideas are proposed to improve the understanding of these reactions.
References
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Journal ArticleDOI

Microwave multicomponent synthesis.

TL;DR: This review will explore the advances and advantages in microwave multicomponent synthesis (MMS) that have been achieved over the last five years.
Journal ArticleDOI

The reaction of (N-isocyanimino)triphenylphosphorane with dialkyl acetylenedicarboxylates in the presence of 1,3-diphenyl-1,3-propanedione: a novel three-component reaction for the stereoselective synthesis of dialkyl (Z)-2-(5,7-diphenyl-1,3,4-oxadiazepin-2-yl)-2-butenedioates

TL;DR: In this article, the reaction of dialkyl (Z)-2-(5,7-diphenyl-1,3,4-oxadiazepin-2-yl)-2-butenedioates with Nisocyaniminotriphenylphosphorane was shown to be completely stereoselective.
Journal ArticleDOI

Synthesis of highly functionalized bis(4H-chromene) and 4H-benzo[g]chromene derivatives via an isocyanide-based pseudo-five-component reaction.

TL;DR: The reactive intermediates generated by the addition of alkyl, aryl, and alicyclic isocyanides to dialkyl acetylenedicarboxylates were trapped to produce highly functionalized bis(4H-chromene)- and 4H-benzo[g]chromene-3,4-dicar boxylate derivatives in fairly good yields in CH(3)CN at room temperature.
Journal ArticleDOI

A grinding-induced catalyst- and solvent-free synthesis of highly functionalized 1,4-dihydropyridines via a domino multicomponent reaction

TL;DR: A grinding-induced catalyst and solvent-free domino multicomponent reaction for the synthesis of 1,4-dihydropyridines has been developed using aldehydes, amines, DEAD (diethyl acetylenedicarboxylate), and malononitrile/ethyl cyanoacetate as discussed by the authors.
Journal ArticleDOI

Three-component synthesis of polysubstituted pyrroles from α-diazoketones, nitroalkenes, and amines.

TL;DR: Polysubstituted pyrroles are regiospecifically synthesized via the copper-catalyzed three-component reaction of α-diazoketones, nitroalkenes, and amines under aerobic conditions.
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