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Showing 1 to 12 of 12 for “"MALONATES"”.

  1. Design, synthesis and evaluation of organocatalysts in 1,4-conjugate additions to nitroolefins and alkylidene malonates

    A family of cinchona-based and thiourea pyrrolidine-based organocatalysts were synthesised and fully characterised. Their catalytic activity and selectivity in 1,4-conjugate additions involving the Michael acceptor, nitrostyrene, was evaluated. Thiourea catalysts based upon the cinchona alkaloid …

    maynooth Repository record for Design, synthesis and evaluation of organocatalysts in 1,4-conjugate additions to nitroolefins and alkylidene malonates (opens in a new tab)

  2. Investigation of artificial malonyl group carriers and multifunctional cyclic scaffolds towards the mimicry of PKS

    … from hydrogen-deuterium exchange experiments of malonates. The results obtained from kinetic experiments allowed us to select the more suitable artificial malonyl carriers in decarboxylative aldol-type condensations. In the second part of the thesis, the first example of a base and metal -free …

    east-anglia Repository record for Investigation of artificial malonyl group carriers and multifunctional cyclic scaffolds towards the mimicry of PKS (opens in a new tab)

  3. Novel aza-arylphosphane ligands for ruthenium catalyzed anti-Markovnikov hydration of terminal alkynes

    … functionalized terminal alkynes, e.g. ketones, malonates, esters. In addition, a new synthetic entry into ß-amino carbonyls has been developed by means of ruthenium-catalyzed anti-MARKOVNIKOV hydration of N-tosyl propargylamines. Finally, the first ruthenium-catalyzed anti-MARKOVNIKOV hydration …

    aachen Repository record for Novel aza-arylphosphane ligands for ruthenium catalyzed anti-Markovnikov hydration of terminal alkynes (opens in a new tab)

  4. New axially chiral amine organocatalysts

    … additions reactions between cyclic enones and malonates, with enantiomeric excesses of 24% seen using optimized conditions.

    east-anglia Repository record for New axially chiral amine organocatalysts (opens in a new tab)

  5. The development and application of metal-catalyzed processes for organic synthesis

    … system for the synthesis of [alpha]-aryl malonates has been developed. Aryl iodides bearing a variety of functional groups can be effectively coupled to diethyl malonate in high yields using inexpensive and widely available reagents, making this a superior method to those previously …

    mit Repository record for The development and application of metal-catalyzed processes for organic synthesis (opens in a new tab)

  6. APPLY LADDER OF CHEMICAL CIRCULARITY: RECYCLING OF RARE EARTH ELEMENTS RECOVERED FROM ELETRONIC WASTE AS A CATALYST IN ORGANIC REACTION.

    … reaction between indoles and benzylidene malonates, employing these catalysts to achieve high reaction efficiency and selectivity. Additionally, a Diels-Alder cycloaddition was performed using chiral auxiliaries, promising results in terms of both reaction yield and enantioselectivity. The …

    milano Repository record for APPLY LADDER OF CHEMICAL CIRCULARITY: RECYCLING OF RARE EARTH ELEMENTS RECOVERED FROM ELETRONIC WASTE AS A CATALYST IN ORGANIC REACTION. (opens in a new tab)

  7. Organocatalytic asymmetric mannich-type reactions: an easy approach to optically active amine derivatives

    … imine precursors and non-commercially available malonates with excellent results in terms of yields and enantioselections.3 In this particular case we recorded 1 mol% of catalyst loading, very low for organocatalytic processes. Then we thought to develop a new Mannich reaction by using simpler …

    bologna Repository record for Organocatalytic asymmetric mannich-type reactions: an easy approach to optically active amine derivatives (opens in a new tab)

  8. Understanding the singlet oxygen reactivity of salarin C through synthesis of a simplified macrocyclic analogue; multicomponent, enantioselective organocatalytic synthesis of tetrahydropyridazinones.

    … from commercially available acid chlorides, malonates and azodicarboxylates. While attempting the oxidation of the N-N bond of the derived tetrahydropyridazinone, an unusual rearrangement to a ketene acetal lactone was also observed. This methodology could be used to construct novel …

    baylor Repository record for Understanding the singlet oxygen reactivity of salarin C through synthesis of a simplified macrocyclic analogue; multicomponent, enantioselective organocatalytic synthesis of tetrahydropyridazinones. (opens in a new tab)

  9. Syntheses of novel acyclic amino-amido ligands

    … (66) from appropriately C-functionalized malonates by amidation with N,N-dimethylethylenediamine (62) followed by reduction of the respective nitro (64) and cyano (63) groups is described. The synthesis of N,N'-bis[2-(N'',N''-dimethylamino)ethyl]iminodiacetamide (73) from diethyl …

    cape-town Repository record for Syntheses of novel acyclic amino-amido ligands (opens in a new tab)

  10. Carbene catalyzed asymmetric nucleophilic acylations with novel triazolium salts

    … addition of heterocyclic aldehydes to arylidene-malonates catalyzed by N-heterocyclic carbenes, which afforded chiral polycarbonyl compounds in good yields (>85%) and good enantioselectivities (up to 78% ee). More importantly, excellent enantiomeric excesses (up to >99% ee) were obtained after …

    aachen Repository record for Carbene catalyzed asymmetric nucleophilic acylations with novel triazolium salts (opens in a new tab)

  11. Novel sulfur containing electrophiles in asymmetric organocatalysis

    … (enamine-catalyzed Michael addition, addition of malonates) were impossible to perform. Moreover, our efforts to perform MBH-reactions with benzaldeyde or Henry reactions with different nitro compounds were unsuccessful. In general, alpha,beta-unsaturated sulfonates were not reactive under various …

    aachen Repository record for Novel sulfur containing electrophiles in asymmetric organocatalysis (opens in a new tab)

  12. ΜΕΛΕΤΗ ΑΝΤΙΔΡΑΣΕΩΝ ΕΤΕΡΟΚΥΚΛΙΚΩΝ ΑΡΩΜΑΤΙΚΩΝ ΝΙΤΡΩΔΑΜΙΝΩΝ

    THE NITROSATION OF 4-METHYLAMINO-1-METHYL-PYRIDINIUM PERCHLORATE IN 0.1-4.0 N PERCHLORIC ACID IS OF FIRST ORDER IN AMINE AND NITROUS ACID AND FOLLOWS THE RATEEXPRESSION: R=K3 [AMINE] [NITROUS ACID] HO. (I) THE RESPECTIVE NITROSAMINE FORMED IS EASILY DENITROSATED UNDER THE EXPERIMENTAL CONDITIONS. …

    greece Repository record for ΜΕΛΕΤΗ ΑΝΤΙΔΡΑΣΕΩΝ ΕΤΕΡΟΚΥΚΛΙΚΩΝ ΑΡΩΜΑΤΙΚΩΝ ΝΙΤΡΩΔΑΜΙΝΩΝ (opens in a new tab)