Results 11 to 20 of about 93,015 (287)

A Microfluidics Reaction System with Automation for a Multicomponent Reaction [PDF]

open access: yesAdvanced Intelligent Systems, 2020
A multicomponent reaction is established toward quinazolimine derivatives, but it requires intensive human interventions in conventional reaction systems to suppress the side reactions. Herein, an automated microfluidics‐based reaction system that uses a
Xinlong Pang, Haoran Zhao, Shaohua Ma
doaj   +3 more sources

Multicomponent Reactions: “Kinderleicht” [PDF]

open access: yesJournal of Chemical Education, 2020
A demonstration experiment of the synthesis of a novel tetrazole derivative via a multicomponent reaction (Ugi tetrazole four component reaction, UT-4CR) bearing a luminol moiety and a subsequent exploitation of its chemiluminescent properties is described.
Constantinos G. Neochoritis   +3 more
openaire   +2 more sources

Pseudo-multicomponent reactions

open access: yesRSC Advances, 2023
Pseudo-MCRs are domino-type one-pot processes that involve combinations of at least three reactants (similarly to normal MCRs) but in which one of them is stoichiometrically duplicated (or more) and hence takes part into two reaction steps (or more).
Julio C. Flores-Reyes   +4 more
openaire   +2 more sources

Multicomponent Reactions [PDF]

open access: yesMolecules, 2019
Multicomponent Reactions appear to be ideal for any form of synthesis, because of their numerous advantages in terms of sustainability and selectivity in building up complex molecular architectures, with high molecular diversity. This Special Issue collects seven contributions which expand our knowledge about Multicomponent Reactions, providing a good ...
openaire   +4 more sources

Multicomponent reactions II [PDF]

open access: yesBeilstein Journal of Organic Chemistry, 2014
The concept of multicomponent reactions (MCR) [1] has been around in organic chemistry since the very early days. Indeed, the first example known in literature, the Strecker synthesis of α-aminonitriles [2], has been developed into an industrial process for the production of methionine in an annual scale of several hundreds of thousand tons per year ...
openaire   +6 more sources

The evaluation of chemoselectivity in multicomponent domino Knoevenagel/Diels-Alder reaction: A DFT study [PDF]

open access: yesJournal of the Serbian Chemical Society, 2021
Herein, the chemoselectivity of the multicomponent domino Knoevenagel/ Diels–Alder reaction is investigated in terms of theoretical calculations. The structures of reagents, transition states, intermediates and products are optimized at the M062X/6-31+G ...
Attarbashi Mina   +2 more
doaj   +1 more source

Ethyl (E)-4-(2,4-Dimethoxyphenyl)-6-(2,4-dimethoxystyryl)-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate

open access: yesMolbank, 2017
A new compound belonging to the “heterostilbene” derivative, namely ethyl (E)-4-(2,4-dimethoxyphenyl)-6-(2,4-dimethoxystyryl)-2-oxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate (2), has been successfully synthesized as an unprecedented side product of the ...
Hery Suwito   +6 more
doaj   +1 more source

From sequence-defined macromolecules to macromolecular pin codes [PDF]

open access: yes, 2020
Dynamic sequence-defined oligomers carrying a chemically written pin code are obtained through a strategy combining multicomponent reactions with the thermoreversible addition of 1,2,4-triazoline-3,5-diones (TADs) to indole substrates.
Badi, Nezha   +4 more
core   +1 more source

Catalyzed and non-catalyzed synthesis of bioactive monastrol

open access: yesQuímica Nova, 2014
The bioactive 3,4-dihydropyrimidin-2(1H)-thione derivative known as Monastrol was synthesized under catalyzed and non-catalyzed conditions through the Biginelli multicomponent reaction under solvent-free conditions.
Haline G. O. Alvim   +4 more
doaj   +1 more source

Stereoselective domino assembling of five molecules: one-pot approach to $(2^\primeR^*,3S^*,4^\primeR^*)$-$2^\prime,4^\prime$-diaryl-$1^\prime,4^\prime$-dihydro-$2^\primeH $-spiro[indoline-$3,3^\prime$-pyridines]

open access: yesComptes Rendus. Chimie, 2020
A new stereoselective multicomponent reaction has been found: domino assembling of two equivalents of benzaldehyde, malononitrile, oxindole and excess of ammonium acetate in acetonitrile resulted in the formation of previously unknown $(2^\primeR^*,3S ...
Ryzhkov, Fedor V.   +5 more
doaj   +1 more source

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