Articles with "enol esters" as a keyword



Copper-Catalyzed Regioselective Olefination and Trifluoromethylation of Carboxylic Acids To Give (Z)-Trifluoromethyl Enol Esters.

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Published in 2022 at "Organic letters"

DOI: 10.1021/acs.orglett.2c02027

Abstract: Herein, we describe a method to produce (Z)-trifluoromethyl enol esters via the olefination and trifluoromethylation of carboxylic acids with TMSCF3. This synthetic method uses inexpensive and easy-to-handle TMSCF3. It employs a commercially available CuCl catalyst… read more here.

Keywords: olefination trifluoromethylation; enol esters; trifluoromethyl enol; carboxylic acids ... See more keywords
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Synthesis of 3-Acyloxyindolenines by TiCl3-Mediated Reductive Cyclization of 2-(ortho-Nitroaryl)-Substituted Enol Esters.

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Published in 2022 at "Organic letters"

DOI: 10.1021/acs.orglett.2c02860

Abstract: In the presence of TiCl3, the reductive cyclization of tetrasubstituted enol esters bearing a 2-(ortho-nitroaryl) substituent affords 3-acyloxy-2,3-disubstituted indolenines in good yields. A domino process involving the partial reduction of nitro to a nitroso group… read more here.

Keywords: reductive cyclization; acyloxyindolenines ticl3; synthesis acyloxyindolenines; ortho nitroaryl ... See more keywords
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Phosphine-Free Ru-Catalyzed Regio- and Stereoselective Addition of Benzoic Acids to Trifluoromethylated Alkynes toward Facile Access to Trifluoromethyl Group-Substituted (E)-Enol Esters

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Published in 2020 at "ACS Omega"

DOI: 10.1021/acsomega.9b03936

Abstract: A combination of ruthenium catalyst with silver salt and copper salt was proved to be a highly efficient protocol for the direct addition reaction of benzoic acids with unsymmetrical trifluoromethylated internal alkynes. Diverse trifluoromethyl group-substituted… read more here.

Keywords: group substituted; addition; trifluoromethyl group; substituted enol ... See more keywords
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Cu(I)-Catalyzed stereoselective synthesis of trisubstituted Z-enol esters via interrupting the 1,3-O-transposition reaction

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Published in 2018 at "Organic chemistry frontiers"

DOI: 10.1039/c8qo00664d

Abstract: An efficient Cu(I)-catalyzed stereoselective synthesis of trisubstituted Z-enol esters via interrupting the 1,3-O-transposition process is reported. This method provided a convenient approach to highly functionalized Z-enol esters with mild reaction conditions and wide substrate scope. read more here.

Keywords: trisubstituted enol; esters via; stereoselective synthesis; catalyzed stereoselective ... See more keywords
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Atom-economic and stereoselective catalytic synthesis of fully substituted enol esters/carbonates of amides in acyclic systems enabled by boron Lewis acid catalysis

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Published in 2023 at "Chemical Science"

DOI: 10.1039/d3sc01394d

Abstract: Carboacyloxylation of internal alkynes is emerging as a powerful and straightforward strategy for enol ester synthesis. However, the reported examples come with limitations, including the utilization of noble metal catalysts, the control of regio- and… read more here.

Keywords: synthesis; enol; lewis acid; enol esters ... See more keywords