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Showing 1 to 20 of 242 for “"Olefins"”.

  1. ORGANOCATALYTIC HALOFUNCTIONALIZATION OF OLEFINS

    Enantioselective halocyclization reactions are important for the synthesis of chiral heterocyclic compounds. In the first part of this thesis, a catalytic enantioselective bromocyclization of olefinic amides has been developed. The resulting enantioenriched 2-substituted 3-bromopiperidines can …

    nus Repository record for ORGANOCATALYTIC HALOFUNCTIONALIZATION OF OLEFINS (opens in a new tab)

  2. Oligomerization of higher olefins

    A series of new substituted cyclopentadienyl ligands and their chromium complexes were successfully synthesised and characterised using a wide range of analytical and spectroscopic techniques such as NMR, mass spectrometry, elemental analysis and melting points.The ligands were then tested for the …

    cape-town Repository record for Oligomerization of higher olefins (opens in a new tab)

  3. Olefins from amine oxides

    Thesis: Ph. D., Massachusetts Institute of Technology, Department of Chemistry, 1957

    mit Repository record for Olefins from amine oxides (opens in a new tab)

  4. Stereoselective Synthesis of Trisubstituted Olefins

    … stereoselective synthesis of trisubstituted olefins is presented. The method involves the stereoselective construction of various $\beta$-hydroxy phosphonamidates followed by their thermolysis to provide trisubstituted olefins in extremely high geometrical purity ($>$99/1).

    uiuc Repository record for Stereoselective Synthesis of Trisubstituted Olefins (opens in a new tab)

  5. Restricted Rotation in Aryl Olefins

    uiuc Repository record for Restricted Rotation in Aryl Olefins (opens in a new tab)

  6. Asymmetric catalytic epoxidations of simple olefins

    Two types of chiral (salen)Mn(III) complexes, either cationic or neutral, were synthesized by complexation of the corresponding chiral salen ligands with manganese salt. Neutral Mn(III) salen complexes were prepared from the ligands and $\rm Mn(OAc)\sb2{\cdot}4H\sb2O$ via in situ aerial oxidation …

    uiuc Repository record for Asymmetric catalytic epoxidations of simple olefins (opens in a new tab)

  7. Oxidative Heck Reactions with Terminal Olefins

    … used to generate branched allylic esters from α-olefins with only the addition of an aryl boronic acid to the reaction mixture. Styrenyl allylic esters are generated in good overall yield and excellent selectivities. The wide functional group tolerance and mild conditions of this three-component …

    uiuc Repository record for Oxidative Heck Reactions with Terminal Olefins (opens in a new tab)

  8. The Ring-opening Polymerisations of Cyclic Olefins

    The ring opening polymerisations of cyclic olefins were investigated using a catalyst system of tungsten hexachloride and aluminium tri-isobutyl. The cyclic olefins investigated were cyclooctene and cyclopentene. The monomers were purified and attempts were made to remove conjugated dienes that …

    aston Repository record for The Ring-opening Polymerisations of Cyclic Olefins (opens in a new tab)

  9. Studies of the sulphation of a-olefins

    … suitable for studying the sulphation of a-Olefins by concentrated sulphuric acid was designed and constructed and its flow characteristics, power consumption and reactor kinetics investigated...

    aston Repository record for Studies of the sulphation of a-olefins (opens in a new tab)

  10. Reactions of phenyl(trihalomethyl)mercurials with olefins

    Thesis: M.S., Massachusetts Institute of Technology, Department of Chemistry, 1964

    mit Repository record for Reactions of phenyl(trihalomethyl)mercurials with olefins (opens in a new tab)

  11. The Study of the Sulphation of [alpha]-olefins

    The sulphation of hexadecene, in concentrated sulphuric acid (98% w/w), has been investigated in a votator scraped-surface heat exchanger reactor with "no-leak". The reactor flow pattern (tangential and axial) has been investigated and the theoretical tangential flow velocity profile determined …

    aston Repository record for The Study of the Sulphation of [alpha]-olefins (opens in a new tab)

  12. New Methods for the Stereoselective Synthesis of Olefins

    Made available in DSpace on 2014-12-10T23:01:44Z (GMT). No. of bitstreams: 1 7412082.pdf: 4063012 bytes, checksum: 607c326a410c5a3da487b28ad2f73993 (MD5) Previous issue date: 1973

    uiuc Repository record for New Methods for the Stereoselective Synthesis of Olefins (opens in a new tab)

  13. Studies on the Stereospecific Synthesis of Trisubstituted Olefins

    Made available in DSpace on 2014-12-10T23:01:46Z (GMT). No. of bitstreams: 1 7412113.pdf: 2628191 bytes, checksum: dda504b7a7be7e1562b8692daed36af3 (MD5) Previous issue date: 1973

    uiuc Repository record for Studies on the Stereospecific Synthesis of Trisubstituted Olefins (opens in a new tab)

  14. Asymmetric hydrogenation of unfunctionalized trisubstituted and tetrasubstituted olefins

    … asymmetric hydrogenation of aryl trisubstituted olefins was generated by combining the complex (EBTHI)MMe2 (EBTHI = ethylenebistetrahydroindenyl, M = Ti, Zr) with [PhMe2NH]+[(BC6F5)4]- under a hydrogen atmosphere. A number of unfunctionalized trisubstituted olefins could be hydrogenated rapidly …

    mit Repository record for Asymmetric hydrogenation of unfunctionalized trisubstituted and tetrasubstituted olefins (opens in a new tab)

  15. Highly Efficient Catalysts for the Dimerization of α-Olefins

    … of my work was the catalytic dimerization of a-olefins, especially the dimerization of propylene. The focus was laid on the optimization of product selectivity, catalyst lifetime, and product separation. Previous studies in our group have shown the enormous potential of bis(imino)pyridin …

    bayreuth Repository record for Highly Efficient Catalysts for the Dimerization of α-Olefins (opens in a new tab)

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