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Published in 2017 at "European Journal of Organic Chemistry"
DOI: 10.1002/ejoc.201601608
Abstract: An efficient palladium-catalyzed nucleophilic substitution/C–H activation/aromatization cascade reaction between readily available 2-halo-N-Ms-arylamines (Ms = methanesulfonyl) and benzyl halides/sulfonates has been described. A wide variety of phenanthridines were synthesized in a one-pot fashion in moderate to…
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Keywords:
halo arylamines;
cascade reaction;
halides sulfonates;
palladium catalyzed ... See more keywords
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Published in 2017 at "Reaction Kinetics, Mechanisms and Catalysis"
DOI: 10.1007/s11144-017-1276-x
Abstract: The synthesized magnetic inorganic–organic hybrid nanocomposite, used as a phase-transfer catalyst on the mesoporous substrate in this paper, provides a green and efficient catalytic system for nucleophilic substitution reactions of benzyl halides in water. The…
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Keywords:
nucleophilic substitution;
microscopy;
substitution reactions;
spectroscopy ... See more keywords
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Published in 2021 at "Organic letters"
DOI: 10.1021/acs.orglett.1c01214
Abstract: A phosphine-catalyzed olefinic cross-coupling between benzyl halides and fumarates is described, which affords trisubstituted alkenes in good yields and excellent E-selectivity under metal-free conditions. Mechanistic studies suggest a catalytic cycle involving phosphorus ylide formation, Michael…
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Keywords:
phosphine catalyzed;
coupling benzyl;
halides fumarates;
cross coupling ... See more keywords
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Published in 2019 at "Organic letters"
DOI: 10.1021/acs.orglett.9b03927
Abstract: Sm(II)-catalyzed carboxylation of benzyl halides is reported through the electrochemical reduction of CO2. The transformation proceeds under mild reaction conditions to afford the corresponding phenylacetic acids in good to excellent yields. This user-friendly and operationally…
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Keywords:
co2;
carboxylation benzyl;
benzyl halides;
activation ... See more keywords
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Published in 2022 at "Chemical communications"
DOI: 10.1039/d1cc05943b
Abstract: 10 mol% B(2,6-C6F2H3)3 in the presence of excess tetramethylpiperidine (TMP) and H2 (or D2) is shown to catalyze the hydrogenative dehalogenation of benzyl-halides to give corresponding toluene derivatives. These reactions proceed via an initial FLP…
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Keywords:
lewis pair;
frustrated lewis;
benzyl;
benzyl halides ... See more keywords