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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…
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Keywords:
ene reactions;
mediated thiol;
reactions organic;
light mediated ... See more keywords
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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…
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Keywords:
trisubstituted cycloalkenes;
ene reactions;
nitrosocarbonyl intermediates;
effect ... See more keywords
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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.
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Keywords:
concerted addition;
ene reactions;
thiol ene;
addition mechanism ... See more keywords
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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),…
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Keywords:
retro ene;
allylic reduction;
ene reactions;
sulfinyl retro ... See more keywords