10 research outputs found

    Winterteelt komkommers, 1961-1962

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    <p><b>Copyright information:</b></p><p>Taken from "Mitochondrial sequences help to resolve deep phylogenetic relationships in rosids"</p><p>http://www.biomedcentral.com/1471-2148/7/217</p><p>BMC Evolutionary Biology 2007;7():217-217.</p><p>Published online 10 Nov 2007</p><p>PMCID:PMC2222252.</p><p></p>rcentages >50. For nodes where ML and MP analyses differ in topology, only the ML BS percentages are shown; asterisks denote contradictory resolutions between ML tree and MP strict consensus of all shortest trees

    Copper-Catalyzed Oxidative Cyclization of Alkynes with Sulfonylhydrazides Leading to 2‑Sulfonated 9<i>H</i>‑pyrrolo­[1,2‑<i>a</i>]­indol-9-ones

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    A copper-catalyzed oxidative cyclization procedure has been developed for the production of 2-sulfonated 9<i>H</i>-pyrrolo­[1,2-<i>a</i>]­indol-9-ones via the direct sulfonylation of <i>N</i>-propargyl-substituted indoles with sulfonyl­hydrazides and <i>tert</i>-butyl hydroperoxide (TBHP). This novel protocol, which tolerates a broad range of functional groups, offers a simple, efficient, and atom-economical route to a series of fluorazones in good yields under mild conditions

    Synthesis of Organophosphorus Compounds through Copper-Catalyzed Annulation Involving C–O and C–P Bond Formations

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    A novel copper­(II) trifluoromethanesulfonate-catalyzed, high-efficiency, and atom-economical synthesis of valuable organophosphorus compounds via cascade annulation of propargylic alcohols with diphenylphosphine oxide is described. This protocol, which has a good functional-group compatibility and insensitivity to an ambient atmosphere, provides a simple and direct pathway to the products, organophosphorus compounds, in good yields under mild conditions. The method could be efficiently scaled up to gram scale, thus highlighting a potential application of this methodology

    Lewis Acid Catalyzed Dehydrogenative Coupling of Tertiary Propargylic Alcohols with Quinoline <i>N</i>‑Oxides

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    An unprecedented Lewis acid catalyzed, high-efficiency synthesis of valuable 2-(quinolin-2-yl)­prop-2-en-1-ones via dehydrogenative coupling of propargylic alkynols with quinoline <i>N</i>-oxides is described. This protocol, which tolerates a broad range of functional groups, provides a straightforward pathway to the products 2-(quinolin-2-yl)­prop-2-en-1-one scaffolds in satisfactory yields. The conversion could be scaled up to gram scale efficiently, which underlines a latent application of this methodology

    Lewis Acid Catalyzed Cyclization of Propargylic Alcohols with 2‑Vinylphenol

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    An unprecedented Lewis acid catalyzed, protection-free, and high-efficiency synthesis of valuable 3,4-dihydro-2<i>H</i>-2,4-methanochromans via cycloaddition of propargylic alkynols with 2-vinylphenol is described. This cycloaddition protocol, which tolerates a wide variety of functional groups, provides practical, versatile, and atom-economical access to a new class of appealing bridged-ring products in satisfactory yields. Compared with the reported reaction conditions for bridged-ring skeletons synthesis, the present reaction conditions are neutral, mild, and without any additives

    AgSCF<sub>3</sub>‑Mediated Trifluoromethylthiolation/Radical Cascade Cyclization of 1,6-Enynes

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    A AgSCF<sub>3</sub>-mediated radical cascade cyclization/trifluoromethylthiolation of 1,6-enynes triggered by a C–C triple bond is developed. This protocol also provides another opportunity to construct a valuable trifluoromethylthio-substituted polycyclic fluorene system through the formations of one C–SCF<sub>3</sub> bond and two C–C bonds in a single step

    BF<sub>3</sub>·OEt<sub>2</sub>‑AgSCF<sub>3</sub> Mediated Trifluoro­methyl­thiolation/Cascade Cyclization of Propynols: Synthesis of 4‑((Trifluoro­methyl)­thio)‑2<i>H</i>‑chromene and 4‑((Trifluoro­methyl)­thio)-1,2-dihydro­quinoline Derivatives

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    A BF<sub>3</sub>·OEt<sub>2</sub>–AgSCF<sub>3</sub> mediated direct trifluoro­methyl­thiolation/cascade cyclization of propynols involving the SCF<sub>3</sub> anion nucleophilic pathway is developed. This protocol also provides an opportunity to construct valuable trifluoromethylthio-substituted 2<i>H</i>-chromene and 1,2-dihydroquinoline systems with high efficiency under mild conditions. Additionally, the developed BF<sub>3</sub>·OEt<sub>2</sub>–AgSCF<sub>3</sub> reaction system could be scaled up to gram quantities in a satisfactory yield without inert gas protection
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