Articles with "ene reactions" as a keyword



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Visible-Light-Mediated Thiol-Ene Reactions through Organic Photoredox Catalysis.

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Published in 2017 at "Organic letters"

DOI: 10.1021/acs.orglett.7b01441

Abstract: Synthetically useful radical thiol-ene reactions can be initiated by visible-light irradiation in the presence of an organic photocatalyst, 9-mesityl-10-methylacridinum tetrafluoroborate. The key thiyl radical intermediates are generated upon quenching of the photoexcited catalyst with a… read more here.

Keywords: ene reactions; mediated thiol; reactions organic; light mediated ... See more keywords
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Ene Reactions of Nitrosocarbonyl Intermediates with Trisubstituted Cycloalkenes: “Cis Effect” and Steric and Conformational Factors Drive the Selectivity

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Published in 2018 at "ACS Omega"

DOI: 10.1021/acsomega.7b01124

Abstract: Nitrosocarbonyl intermediates, generated at room temperature by oxidation of nitrile oxides, undergo clean ene reactions with trisubstituted cycloalkenes. Nitrosocarbonyl benzene follows a Markovnikov orientation and abstracts preferentially the twix hydrogens over the lone ones. With… read more here.

Keywords: trisubstituted cycloalkenes; ene reactions; nitrosocarbonyl intermediates; effect ... See more keywords
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A concerted addition mechanism in [Hmim]Br-triggered thiol–ene reactions: a typical “ionic liquid effect” revealed by DFT and experimental studies

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Published in 2019 at "New Journal of Chemistry"

DOI: 10.1039/c8nj05674a

Abstract: The π+–π and H-bond interactions between [Hmim]Br and substrates promote a special one-step addition mechanism in thiol–ene reactions. read more here.

Keywords: concerted addition; ene reactions; thiol ene; addition mechanism ... See more keywords
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Stereoselective allylic reduction via one-pot palladium-catalyzed allylic sulfonation and sulfinyl retro-ene reactions

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Published in 2018 at "Organic chemistry frontiers"

DOI: 10.1039/c8qo00233a

Abstract: A tandem approach for the stereoselective allylic reduction has been developed based on a strategy combining the palladium-catalyzed S-allylation and the sulfinyl retro-ene reactions. In a one-pot process employing various allylic carbonates, sodium t-butyldimethylsilyloxymethanesulfinate (TBSOMS-Na),… read more here.

Keywords: retro ene; allylic reduction; ene reactions; sulfinyl retro ... See more keywords