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Published in 2017 at "Chemistry of Heterocyclic Compounds"
DOI: 10.1007/3585
Abstract: We present a comprehensive analysis of data published over the last decade about the methods applicable to the synthesis of fused polyheterocyclic compounds on the basis of glycolurils. Authors: Yana A. Barsegyan*, Vladimir V. Baranov,…
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Keywords:
polyheterocyclic compounds;
glycolurils synthesis;
fused polyheterocyclic;
compounds glycolurils ... See more keywords
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Published in 2017 at "Chemistry of Heterocyclic Compounds"
DOI: 10.1007/s10593-017-2029-5
Abstract: We present a comprehensive analysis of data published over the last decade about the methods applicable to the synthesis of fused polyheterocyclic compounds on the basis of glycolurils.
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Keywords:
polyheterocyclic compounds;
glycolurils synthesis;
fused polyheterocyclic;
compounds glycolurils ... See more keywords
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Published in 2018 at "Tetrahedron Letters"
DOI: 10.1016/j.tetlet.2018.10.017
Abstract: Abstract In this paper, we have described a simple and efficient strategy for the synthesis of fused pyrazole derivatives. The key steps of our strategy involves hydroamination, copper-catalyzed cross dehydrogenative coupling (CDC) followed by aromatization…
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Keywords:
pyrazole derivatives;
fused pyrazole;
strategy;
synthesis fused ... See more keywords
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Published in 2023 at "Organic letters"
DOI: 10.1021/acs.orglett.3c01466
Abstract: A facile and straightforward approach for the synthesis of fused quinoxalinones via palladium-catalyzed cascade carbonylative cyclization of 2-heteroaryl iodobenzene and NaN3 has been achieved. The transformation might undergo cascade carbonylation, formation of acyl azide, a…
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Keywords:
quinoxalinones via;
palladium catalyzed;
synthesis fused;
fused quinoxalinones ... See more keywords
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Published in 2021 at "ACS Omega"
DOI: 10.1021/acsomega.1c01466
Abstract: A method for the synthesis of fused 1,3-dioxolanes was developed by self-condensation of glyoxal generated in situ by oxidation of acetophenones with SeO2 in the presence of trifluoroacetic acid. Three molecules of the glyoxal generated…
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Keywords:
synthesis fused;
self condensation;
trifluoroacetic acid;
presence ... See more keywords
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Published in 2017 at "Green Chemistry"
DOI: 10.1039/c6gc01553k
Abstract: Benzyl bromides bearing an ortho-substituted α,β-unsaturated ketone moiety are found to be promising precursors for the synthesis of fused 1,2,3-triazole and isoindoline derivatives via an intramolecular azide–alkene cascade reaction under catalyst free conditions. Fused 1,2,3-triazole…
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Keywords:
fused triazole;
isoindoline derivatives;
triazole isoindoline;
reaction ... See more keywords
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Published in 2023 at "Chemical communications"
DOI: 10.1039/d2cc05831f
Abstract: Herein, we disclose the first report on the generation of cyanonitrone in situ from diazoacetonitrile and nitrosoarene, and its subsequent [3+2] cycloaddition with oxabicyclic alkenes to access fused tricyclic cyanoisoxazolidines. Further, this methodology could be…
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Keywords:
situ;
additive free;
synthesis fused;
fused tricyclic ... See more keywords
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Published in 2023 at "Chemical communications"
DOI: 10.1039/d3cc01920a
Abstract: An NBS-induced intramolecular annulation of 3-(1H-indol-3-yl)-N-alkoxypropanamide is described. The reactions proceed well and quickly under mild conditions with the help of a base. It was found that C2-substituents on the indole ring in 3-(1H-indol-3-yl)-N-alkoxypropanamide have…
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Keywords:
nbs induced;
intramolecular annulation;
induced intramolecular;
divergent synthesis ... See more keywords
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Published in 2023 at "Chemical Science"
DOI: 10.1039/d3sc00118k
Abstract: Highly diastereo-/enantioselective assembly of 2,3-fused indolizine derivatives could be easily available through a cascade allylation/Friedel–Crafts type reaction enabled by a synergistic Cu/Ir catalysis. This designed protocol provides an unprecedented and facile route to enantioenriched indolizines…
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Keywords:
diastereodivergent synthesis;
synthesis fused;
enantio diastereodivergent;
synergistic catalysis ... See more keywords
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Published in 2020 at "Synlett"
DOI: 10.1055/s-0040-1705960
Abstract: A convenient process is described for the synthesis of novel thiazolo[4,5-b]pyridines fused with triazole or pyrimidine rings. The base-promoted reactions of 2-chloro-3-nitropyridines with 1,3-(S,N)-binucleophiles (triazole-5-thiols, 4-oxopyrimidine-2-thiones) resulted in nucleophilic substitution of the chlorine atom and…
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Keywords:
thiazolo pyridines;
fused thiazolo;
pyridines successive;
simple synthesis ... See more keywords
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Published in 2018 at "Synthetic Communications"
DOI: 10.1080/00397911.2018.1448419
Abstract: ABSTRACT A novel synthesis of N-fused imino-1,2,4-thiadiazolo derivatives is described. This approach involves the inexpensive, nontoxic, recoverable, and easy to handle montmorillonite K10 that catalyzes the coupling of 3-aminoisoquinolines and phenylisothiocyanates to afford the N-fused…
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Keywords:
synthesis fused;
montmorillonite k10;
fused imino;
imino thiadiazolo ... See more keywords