PIDA-mediated intramolecular oxidative C–N bond formation for the direct synthesis of quinoxalines from enaminones
نویسندگان
چکیده
منابع مشابه
nano-rods zno as an efficient catalyst for the synthesis of chromene phosphonates, direct amidation and formylation of amines
چکیده ندارد.
Aqua mediated SnO2 nanoparticles: A recyclable and benign catalyst for the synthesis of Quinoxalines
An efficient and mild synthesis of quinoxalines in cludingcyclo-condensation of 1, 2-phenylenediamine and 1, 2-diketonesin the presence of1mol% catalytic amount of SnO2 nanoparticles (1 mol%) in water at room temperature is established. On the whole, this study introduced at this point is substantial in terms of using water as solvent, low reaction time (5 to 10 minutes), high yields...
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Correction for 'Copper-catalyzed, hypervalent iodine mediated C=C bond activation of enaminones for the synthesis of α-keto amides' by Jie-Ping Wan et al., Chem. Commun., 2016, 52, 1270-1273.
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An efficient iodine-mediated oxidative annulation of aryl acetylenes-arylethenes-aromatic ketones with 1,2-diamines for the synthesis of pyrazines and regioselective synthesis of quinoxalines is presented. A multipathway coupled domino approach has been developed for the one-pot synthesis of 1,4-diazines with high functional group compatibility.
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An efficient and exceptionally mild intramolecular nickel-catalyzed carbon-oxygen bond-forming reaction between vinyl halides and primary, secondary, and tertiary alcohols has been achieved. Zinc powder was found to be an essential additive for obtaining high catalyst turnover and yields. This operationally simple method allows direct access to cyclic vinyl ethers in high yields in a single step.
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ژورنال
عنوان ژورنال: RSC Advances
سال: 2019
ISSN: 2046-2069
DOI: 10.1039/c9ra01200a