421 research outputs found

    Modification of the Directive Influence of Substituents in Certain Benzene Derivatives

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    Bromination of vanillin, 3-methoxy-4-hydroxybenzaldehyde, gives a yield of 88-90 per cent of the 5-bromo compound which indicates that the chief directive influence is exerted by hydroxyl. If the hydroxyl radical is first acylated and the resulting acetyl or benzoyl vanillin is brominated, an equally high yield of the 6-bromo derivative is obtained, and no other product can be isolated. Vanillic acid and methyl vanillate likewise give good yields of the corresponding 5-bromo compounds, while the acylated derivatives give the 6-bromo substitution products only. These results indicate that acylation of hydroxyl suppresses its orienting effect and the entrance of bromine into position 6 shows that the methoxy radical then exercises the chief directive influence

    Chemo- and enantioselective sulfoxidation of bis(ethylenedithio)-tetrathiafulvalene (BEDT-TTF) into chiral BEDT-TTF-sulfoxide

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    Selective sulfoxidation of BEDT-TTF (bis(ethylenedithio)-tetrathiafulvalene) with enantiopure (camphoryl-sulfonyl)oxaziridine derivatives provided the inner monosulfoxide, as demonstrated using single crystal X-ray analysis, with an enantiomeric excess of 44% (up to 74% after recrystallization)

    Steric Hindrance in the Behavior of Phenyl Alkyl Ether and Derivatives

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    It is known that phenyl alkyl ethers substitute in the phenyl radical less easily than phenol; nevertheless, phenetol will give a tribromophenyl compound. When the allyl derivative is used, both phenyl and allyl radicals may be involved in the change. Experiments now in progress show that rearrangement of the allyl ether by heat, according to Claisen\u27s method may cause a loss of bromine

    A Smile, A Kiss And You

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    https://digitalcommons.library.umaine.edu/mmb-vp/4555/thumbnail.jp

    Let Me Go Back

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    https://digitalcommons.library.umaine.edu/mmb-vp/3246/thumbnail.jp

    The Cosmic Coincidence as a Temporal Selection Effect Produced by the Age Distribution of Terrestrial Planets in the Universe

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    The energy densities of matter and the vacuum are currently observed to be of the same order of magnitude: (Ωm0≈0.3)∼(ΩΛ0≈0.7)(\Omega_{m 0} \approx 0.3) \sim (\Omega_{\Lambda 0} \approx 0.7). The cosmological window of time during which this occurs is relatively narrow. Thus, we are presented with the cosmological coincidence problem: Why, just now, do these energy densities happen to be of the same order? Here we show that this apparent coincidence can be explained as a temporal selection effect produced by the age distribution of terrestrial planets in the Universe. We find a large (∼68\sim 68 %) probability that observations made from terrestrial planets will result in finding Ωm\Omega_m at least as close to ΩΛ\Omega_{\Lambda} as we observe today. Hence, we, and any observers in the Universe who have evolved on terrestrial planets, should not be surprised to find Ωm∼ΩΛ\Omega_m \sim \Omega_{\Lambda}. This result is relatively robust if the time it takes an observer to evolve on a terrestrial planet is less than ∼10\sim 10 Gyr.Comment: Submitted to Ap

    Arc Operads and Arc Algebras

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    Several topological and homological operads based on families of projectively weighted arcs in bounded surfaces are introduced and studied. The spaces underlying the basic operad are identified with open subsets of a compactification due to Penner of a space closely related to Riemann's moduli space. Algebras over these operads are shown to be Batalin-Vilkovisky algebras, where the entire BV structure is realized simplicially. Furthermore, our basic operad contains the cacti operad up to homotopy, and it similarly acts on the loop space of any topological space. New operad structures on the circle are classified and combined with the basic operad to produce geometrically natural extensions of the algebraic structure of BV algebras, which are also computed.Comment: Published by Geometry and Topology at http://www.maths.warwick.ac.uk/gt/GTVol7/paper15.abs.htm

    Brother\u27s Lullaby

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    https://digitalcommons.library.umaine.edu/mmb-vp/5256/thumbnail.jp
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