https://lnkd.in/e4qAX4rU A mild and practical protocol for the copper-mediated trifluoromethylation of aryl and heteroaryl boronic acids
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Professor of Chemistry at University of Bologna, Associate Editor at Chemical Science (RSC)
If you need a method to synthesize aryl alkyl thioethers avoiding thiols (and related unpleasant odor and air instability), you may want to check out our photochemical organocatalytic protocol that stitches together inexpensive alcohols and aryl chlorides https://lnkd.in/dVmn_vih
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An interesting method for the preparation of thioethers without the smell of thiols!
Professor of Chemistry at University of Bologna, Associate Editor at Chemical Science (RSC)
If you need a method to synthesize aryl alkyl thioethers avoiding thiols (and related unpleasant odor and air instability), you may want to check out our photochemical organocatalytic protocol that stitches together inexpensive alcohols and aryl chlorides https://lnkd.in/dVmn_vih
Photochemical Organocatalytic Synthesis of Thioethers from Aryl Chlorides and Alcohols
pubs.acs.org
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https://lnkd.in/eKrT5EzA A mild and practical protocol for the copper-mediated trifluoromethylation of aryl and heteroaryl boronic acids
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In this application note, learn how Cyanidin-3-glucoside can be extracted from black rice and purified with a prepLC/Flash system quickly and easily, from rapid ID to intelligent method development using the following prep-free technology: 1) The AVANT® (U)HPLC and expression® CMS for LC-UV-MS Analysis, Purity Analysis and Confirmation. 2) The Puri Flash® 5.250 for separation and purification of the black rice.
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https://lnkd.in/eF8yPdQ5 A highly efficient, practical, and ligand-free palladium-catalyzed carbonylation of aryl iodides with alkenylboronic acids
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https://lnkd.in/geJyNtpq A practical tandem condensation N-alkylation reaction has been developed for trisubstituted hydrazone formation using aldehydes, hydrazines, and alkyl halides. This method addresses chemoselectivity issues, enabling one-pot reactions with diverse functional groups including halo- and heterofunctional groups, as well as free hydroxyl and amino groups. The process yields a wide range of trisubstituted hydrazones in good to excellent yields.
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https://lnkd.in/eS9-YQfY DMAP catalyzes a controllable, base-free, decarboxylative isocyanation of carboxylic acids with 1,1-dimethyl-2,2,2-trichloroethoxycarbonyl azide
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https://lnkd.in/g3tfBuDv A photocatalytic decarboxylation of α,β-unsaturated acids followed by a C-O cross-coupled esterification provides α-oxycarbonyl-β-ketones.
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