Articles with "derivatives via" as a keyword



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A novel access to 4-trifluoromethyl-1,3-thiazole derivatives via an intermediate thiocarbonyl ylide

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Published in 2019 at "Journal of Fluorine Chemistry"

DOI: 10.1016/j.jfluchem.2019.02.003

Abstract: Abstract A Lewis acid catalyzed reaction of trifluoroacetyldiazomethane (CF3COCHN2) with thiourea occurs in boiling THF solution in the presence of BF3·OEt2 yielding 2-amino-4-trifluoromethyl-1,3-thiazole in a fair yield. Analogous reactions with aromatic thioamides, performed in the… read more here.

Keywords: trifluoromethyl thiazole; thiazole derivatives; access trifluoromethyl; derivatives via ... See more keywords
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Highly efficient CuOx/OMS-2 catalyst for synthesis of phenoxathiin derivatives via intramolecular arylations of phenols with aryl halides

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Published in 2019 at "Tetrahedron Letters"

DOI: 10.1016/j.tetlet.2019.151259

Abstract: Abstract Phenoxathiin and its derivatives have attracted a great deal of interest due to their unique chemical and physical properties and their applications in fluorescent materials, antifungal activities and selective inhibitors. In the presence of… read more here.

Keywords: phenoxathiin derivatives; via intramolecular; arylations phenols; intramolecular arylations ... See more keywords
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Transformations of Less-Activated Phenols and Phenol Derivatives via C-O Cleavage.

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Published in 2020 at "Chemical reviews"

DOI: 10.1021/acs.chemrev.0c00088

Abstract: Employing phenols and phenol derivatives as electrophiles for cross-coupling reactions has numerous advantages over commonly used aryl halides in terms of environmental-friendliness and sustainability. In the early stage of discovering such transformations, most efforts have… read more here.

Keywords: phenol derivatives; phenols phenol; transformations less; activated phenols ... See more keywords
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Synthesis of 2-Cyanomethyl Indane Derivatives via Pd-Catalyzed Alkene Difunctionalization Reactions of Alkyl Nitriles.

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Published in 2023 at "Organic letters"

DOI: 10.1021/acs.orglett.3c00571

Abstract: The synthesis of indanes bearing substituted cyanomethyl groups at C2 is achieved through Pd-catalyzed coupling reactions between 2-allylphenyl triflate derivatives and alkyl nitriles. Related partially saturated analogues were generated from analogous transformations of alkenyl triflates.… read more here.

Keywords: cyanomethyl indane; alkyl nitriles; synthesis cyanomethyl; via catalyzed ... See more keywords
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Mild Functionalization of Tetraoxane Derivatives via Olefin Metathesis: Compatibility of Ruthenium Alkylidene Catalysts with Peroxides.

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Published in 2017 at "Organic letters"

DOI: 10.1021/acs.orglett.6b03688

Abstract: An easy and mild functionalization method of tetraoxane derivatives via olefin metathesis is reported. This reaction offers a new method to afford fully functionalized tetraoxanes in high yields. This method is also utilized in the… read more here.

Keywords: via olefin; derivatives via; mild functionalization; olefin metathesis ... See more keywords
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Synthesis of Difluoroalkylated Benzofuran, Benzothiophene, and Indole Derivatives via Palladium-Catalyzed Cascade Difluoroalkylation and Arylation of 1,6-Enynes.

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Published in 2020 at "Organic letters"

DOI: 10.1021/acs.orglett.9b04681

Abstract: A novel and efficient method for the synthesis of difluoroalkylated benzofuran, benzothiophene, and indole derivatives via palladium-catalyzed aryldifluoroalkylation of 1,6-enynes with ethyl difluoroiodoacetate and arylboronic acids has been established. High reaction efficiency, mild conditions, broad… read more here.

Keywords: benzofuran benzothiophene; difluoroalkylated benzofuran; synthesis difluoroalkylated; indole derivatives ... See more keywords
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Synthesis of Benzoazepine Derivatives via Azide Rearrangement and Evaluation of Their Antianxiety Activities.

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Published in 2021 at "ACS medicinal chemistry letters"

DOI: 10.1021/acsmedchemlett.1c00275

Abstract: A new synthetic method for the construction of benzoazepine analogues has been developed employing ortho-arylmethylbenzyl azide derivatives as precursors using an azide rearrangement reaction. In this work, 14 benzoazepine compounds were successfully synthesized in moderate… read more here.

Keywords: antianxiety; synthesis benzoazepine; via azide; benzoazepine derivatives ... See more keywords
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Facile Route to the Synthesis of 1,3-Diazahetero-Cycle-Fused [1,2-a]Quinoline Derivatives via Cascade Reactions

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Published in 2018 at "ACS Omega"

DOI: 10.1021/acsomega.7b01856

Abstract: A one-step protocol without transition-metal catalysts with simple post-treatment for the synthesis of 1,3-diazaheterocycle-fused [1,2-a]quinoline derivatives via the cascade reaction of 2-fluorobenzaldehyde (1) and heterocyclic ketene aminals (2) was developed. In the one-step cascade reaction,… read more here.

Keywords: via cascade; facile route; fused quinoline; derivatives via ... See more keywords
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Enantioselective Synthesis of α-Aminoboronic Acid Derivatives via Copper-Catalyzed N-Alkylation.

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Published in 2023 at "Journal of the American Chemical Society"

DOI: 10.1021/jacs.3c00038

Abstract: Due to burgeoning interest in the pharmaceutical industry in exploiting optically active α-aminoboronic derivatives as bioisosteres of α-amino acid derivatives, the discovery of methods for their catalytic asymmetric synthesis is an important challenge. Herein, we… read more here.

Keywords: synthesis aminoboronic; copper; enantioselective synthesis; synthesis ... See more keywords
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Synthesis of pertrifluoromethyl pyridazine derivatives via a tandem reaction of aryldiazonium salts with hexafluoroacetylacetone

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Published in 2020 at "Organic Chemistry Frontiers"

DOI: 10.1039/d0qo00955e

Abstract: A method for the synthesis of pertrifluoromethyl pyridazine derivatives by the condensation of arenediazonium salts with hexafluoroacetylacetone has been developed. read more here.

Keywords: salts hexafluoroacetylacetone; pyridazine derivatives; derivatives via; pertrifluoromethyl pyridazine ... See more keywords
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Preparation of 2′-Alkylselenouridine Derivatives via a 2-(Trimethyl­silyl)ethylselenation Approach

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Published in 2017 at "Synlett"

DOI: 10.1055/s-0036-1588937

Abstract: 2′-O-Methylation of nucleotides is well-known to increase siRNA stability against nuclease activities. Recently, selenium-containing biomolecules have been recognized as unique biological and medicinal agents for humans. In this study, 2′-alkylselenouridine derivatives were prepared through 2-(trimethylsilyl)ethylselenation… read more here.

Keywords: alkylselenouridine derivatives; via trimethyl; ethylselenation; derivatives via ... See more keywords