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Published in 2021 at "Journal of the American Chemical Society"
DOI: 10.1021/jacs.1c09489
Abstract: Selective hydrogenation of alkynes to alkenes requires a catalytic site with suitable electronic properties for modulating the adsorption and conversion of alkyne, alkene as well as dihydrogen. Here, we report a complex palladium hydride, CaPdH2,…
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Keywords:
alkynes alkenes;
semihydrogenation alkynes;
hydride;
enabling semihydrogenation ... See more keywords
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Published in 2018 at "Green Chemistry"
DOI: 10.1039/c7gc03175k
Abstract: Bronsted acid-catalyzed cyclization reactions of N-alkyl anilines with alkynes or alkenes in the presence of oxygen gas as an oxidant under metal- and solvent-free conditions are described. Various quinoline derivatives are obtained in satisfactory to…
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Keywords:
alkynes alkenes;
alkyl anilines;
metal solvent;
acid catalyzed ... See more keywords
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Published in 2020 at "Organic chemistry frontiers"
DOI: 10.1039/d0qo00339e
Abstract: An addition reaction of pyridine-tetrafluoro-λ6-sulfanylchlorides (Py-SF4Cl) to alkynes and alkenes providing pyridine-tetrafluoro-λ6-sulfanyl-alkenes and pyridine-tetrafluoro-λ6-sulfanyl-alkanes is represented. The addition of Py-SF4Cl occurs spontaneously in the presence of reactants, even in total darkness, but is affected in…
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Keywords:
alkynes alkenes;
tetrafluoro sulfanyl;
addition;
presence ... See more keywords
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Published in 2018 at "Molecules"
DOI: 10.3390/molecules24010101
Abstract: Diboron reagents have been traditionally regarded as “Lewis acids”, which can react with simple Lewis base to create a significant nucleophilic character in one of boryl moieties. In particular, bis(pinacolato)diboron (B2pin2) reacts with simple Lewis…
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Keywords:
alkynes alkenes;
organoboron compounds;
free catalytic;
recent synthesis ... See more keywords