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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 2022 at "ACS Omega"
DOI: 10.1021/acsomega.1c06216.s001
Abstract: An efficient and green route of C–C bond formation was disclosed to construct 2,3-diaryl-1,4-diketones from α-methylene ketones by the catalysis of tetrabutylammonium iodide (TBAI) with tert-butyl hydroperoxide (TBHP) as an oxidant in water. This reaction…
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Keywords:
catalyzed oxidative;
diaryl diketones;
water;
coupling benzyl ... See more keywords
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Published in 2022 at "Journal of the American Chemical Society"
DOI: 10.1021/jacs.2c00957
Abstract: The enantioconvergent radical C(sp3)-C(sp2) cross-coupling of alkyl halides with alkenylboronate esters is an appealing tool in the assembly of synthetically valuable enantioenriched alkenes owing to the ready availability, low toxicity, and air/moisture stability of alkenylboronate…
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Keywords:
enantioconvergent radical;
coupling benzyl;
cross coupling;
halides alkenylboronate ... See more keywords