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Showing 1 to 10 of 10 for “"asymmetric hydrogenation"”.

  1. Asymmetric hydrogenation catalysed by platinum and iridium

    The enantioselective hydrogenation of α-ketoesters over supported platinum metal catalysts which have been modified by chiral molecules has been studied. The aim of this thesis was (a) to gain a greater understanding of the kinetics of asymmetric hydrogenation of methyl pyruvate (MeCOCOOMe) to …

    hull Repository record for Asymmetric hydrogenation catalysed by platinum and iridium (opens in a new tab)

  2. Asymmetric hydrogenation of unfunctionalized trisubstituted and tetrasubstituted olefins

    A highly reactive chiral catalyst for the 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 …

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

  3. Novel Metal Amido-Complexes – Syntheses, Reactivity and Asymmetric Catalysis

    … high selectivities and good activities in the asymmetric hydrogenation of ketones, the development of amido-complex catalysts for the enantioselective hydrogenation of imines represents a major focus of this work. A library of novel amines 4 was synthesized by deprotonation of the hydroxyl …

    bayreuth Repository record for Novel Metal Amido-Complexes – Syntheses, Reactivity and Asymmetric Catalysis (opens in a new tab)

  4. Water Soluble Phosphines, Their Transitional Metal Complexes, and Catalysts

    … phosphine analog. Finally, homogeneous asymmetric hydrogenation was carried out in the presence of a chiral surfactant in an attempt to affect asymmetric induction. The catalytic results showed that at a surfactant/Rh ratio of 25, the asymmetric hydrogenation of AACA-Me …

    vt Repository record for Water Soluble Phosphines, Their Transitional Metal Complexes, and Catalysts (opens in a new tab)

  5. DFT Studies of the Organocatalytic Aldol Reaction and a Frustrated Lewis Pair

    … Lewis pair based on a chiral backbone for the asymmetric hydrogenation of imines and enamines was designed and the ability of hydrogen splitting by this new FLP system was examined by computational modeling and calculating the hydrogen activation energy barrier.

    brock Repository record for DFT Studies of the Organocatalytic Aldol Reaction and a Frustrated Lewis Pair (opens in a new tab)

  6. Synthesis and application of pinene-pyridine derivatives in asymmetric catalysis

    … derivatives, and their application in asymmetric catalysis. Both transition metal catalysed and organocatalytic transformations were investigated. Chiral pyridine-phosphines based on α-pinene were synthesised and applied as efficient P,N-ligands for the enantioselective …

    glasgow Repository record for Synthesis and application of pinene-pyridine derivatives in asymmetric catalysis (opens in a new tab)

  7. Accelerating process development of complex chemical reactions

    … Our case study was a homogeneous Rh-catalysed asymmetric hydrogenation to produce a chiral γ-lactam, with conversion and diastereoselectivity as objectives. We adapted a state-of-the-art multi-objective machine learning algorithm, based on Gaussian processes, to utilise the descriptors as …

    cambridge Repository record for Accelerating process development of complex chemical reactions (opens in a new tab)

  8. Accessing Challenging Fluorinated Motifs Using Photoredox Catalysis And Enabling Technologies

    … small molecules has resulted in the pursuit of asymmetric hydrogenation of α–trifluoromethylalkenes to access chiral trifluoromethyl alkane products. This work has been enabled by the co-development of a new analytical technique, molecular rotational resonance spectroscopy, which enables the …

    penn Repository record for Accessing Challenging Fluorinated Motifs Using Photoredox Catalysis And Enabling Technologies (opens in a new tab)