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Showing 1 to 20 of 32 for “"[2+2]-Cycloaddition"”.

  1. Synthesis of 3-aminocyclobutenones via [2 + 2] cycloaddition of ynamides and ketenes

    … classes of ketenes in intermolecular [2 + 2] cycloaddition to afford substituted cyclobutenones with complete regioselectivity. The cycloaddition substrates are easily assembled from amine derivatives by copper-catalyzed N-alkynylation with acetylenic bromides. The alkynylation reaction …

    mit Repository record for Synthesis of 3-aminocyclobutenones via [2 + 2] cycloaddition of ynamides and ketenes (opens in a new tab)

  2. Stereoselective Intramolecular Rhodium(I)-Catalyzed [(3+2+2)] Cycloaddition Reactions of Alkylidenecyclopropanes (ACPs) for the Concise Synthesis of Bridged Tricyclic Products

    Transition metal-catalyzed higher-order [m+n+o] cycloadditions are an important class of reactions for constructing elaborate carbocycles and heterocycles in a highly convergent manner. In particular, cycloadditions with alkylidenecyclopropanes (ACPs) as three-carbon synthons offer a versatile …

    queens Repository record for Stereoselective Intramolecular Rhodium(I)-Catalyzed [(3+2+2)] Cycloaddition Reactions of Alkylidenecyclopropanes (ACPs) for the Concise Synthesis of Bridged Tricyclic Products (opens in a new tab)

  3. CRYSTAL ENGINEERING STUDIES ON THE MOLECULAR SALTS AND SILVER(I) COORDINATION COMPOUNDS FOR [2+2] CYCLOADDITION REACTION IN THE SOLID STATE

    … analysed in terms of their solid state [2 + 2] cycloaddition reaction to synthesize a particular isomer of the corresponding cyclobutane compounds. The crucial role of the anions in the selective preorganization before photodimerization and the acid catalysed isomerisation of the cyclobutane …

    nus Repository record for CRYSTAL ENGINEERING STUDIES ON THE MOLECULAR SALTS AND SILVER(I) COORDINATION COMPOUNDS FOR [2+2] CYCLOADDITION REACTION IN THE SOLID STATE (opens in a new tab)

  4. I. [2 +2] Cycloaddition and benzannulation of 2-iodoynamides and application to the construction of highly substituted indoles : II. Synthesis of furo[2,3-g]thieno[2,3-e]indole via a benzannulation strategy

    … undergo efficient and regioselective [2 + 2] cycloaddition with ketene to produce cyclobutenones that are useful synthetic building blocks. Reaction of 2-iodoynamides and vinylketenes generated in situ from cyclobutenones proceeds via a pericyclic cascade mechanism to produce highly …

    mit Repository record for I. [2 +2] Cycloaddition and benzannulation of 2-iodoynamides and application to the construction of highly substituted indoles : II. Synthesis of furo[2,3-g]thieno[2,3-e]indole via a benzannulation strategy (opens in a new tab)

  5. Typselektivität und Diastereoselektivität in den Oxidationen von chiralen oxazolidinonsubstituierten Encarbamaten mit Singulettsauerstoff, Dimethyldioxiran und meta-Chlorperbenzoesäure

    … die Typselektivität (En-Reaktion versus [2+2]-Cycloaddition) kontrolliert. Bei der [2+2]-Cycloaddition der Encarbamate I mit Singulettsauerstoff (1O2) und der Epoxidierung mit DMD und mCPBA wurden hohe Diastereoselektivitäten beobachtet. Die folgenden Ergebnisse wurden erzielt: 1. Die …

    wurz-thes Repository record for Typselektivität und Diastereoselektivität in den Oxidationen von chiralen oxazolidinonsubstituierten Encarbamaten mit Singulettsauerstoff, Dimethyldioxiran und meta-Chlorperbenzoesäure (opens in a new tab)

  6. Development of Nickel and Zirconium Mediated Cycloadditions for the Synthesis of Substituted Pentacene

    The regioselectivity of the [2+2+2] cycloaddition of nickel-benzynes and 1,3-diynes could be maintained when asymmetrically substituted 1,3-diynes were employed. The ability to incorporate an asymmetric 1,3-diyne into the oligoacene backbone provided substituents that could be differentiated in …

    uiuc Repository record for Development of Nickel and Zirconium Mediated Cycloadditions for the Synthesis of Substituted Pentacene (opens in a new tab)

  7. Regio- und stereoselektive Synthese von Sesquiterpenen und hormonell aktiven Cholesterinderivaten

    … wird die Anwendung der Lewis-Säure vermittelten Cycloadditionen von Allylsilanen an alpha,beta-ungesättigte Carbonylverbindungen beschrieben. Das Sesquiterpen Isocomen wurde unter Anwendung der [3+2]-Cycloaddition an Enone synthetisch hergestellt. Die [2+2]-Cycloaddition an Acrylsäurederivate …

    qucosa-diss

  8. Synthesis of Aryl Ynol Ethers and Their Synthetic Applications

    … Moreover, we discovered a hetero-[2+2]-cycloaddition reaction between aryl ketenes and aryl ynol ethers, and the forming cyclobutenones could undergo a retro-4π/6π electrocyclization reaction to afford naphthlenes. Finally, we utilized this novel electrocyclization in the synthesis of …

    utswmed Repository record for Synthesis of Aryl Ynol Ethers and Their Synthetic Applications (opens in a new tab)

  9. Preparation of benzoenyne -allenes, enyne -isocyanates and enyne -carbodiimides and their applications in the synthesis of polycyclic aromatic hydrocarbons and heterocycles

    … in certain cases the intramolecular [2+2] cycloaddition reaction of the chlorinated benzoenyne-allene intermediates occurred preferentially to form 1H-cyclobut[a]indenes. Competition from the intramolecular [2+2] cycloaddition reaction could be avoided with the non-chlorinated …

    wvu Repository record for Preparation of benzoenyne -allenes, enyne -isocyanates and enyne -carbodiimides and their applications in the synthesis of polycyclic aromatic hydrocarbons and heterocycles (opens in a new tab)

  10. Strategies for the synthesis of bioactive compounds: biomimetic approaches to the Salinosporamides and the hexadehydro-Diels-Alder reaction

    … uncatalyzed intramolecular ketene-ketone [2+2] cycloaddition of an amidoketene precursor. We also propose a transition state that places the C2 substituent pseudo-equatorial, allowing for enhanced stereoselectivity during bis-cyclization. Enolate formation from a thioester followed by internal …

    umn Repository record for Strategies for the synthesis of bioactive compounds: biomimetic approaches to the Salinosporamides and the hexadehydro-Diels-Alder reaction (opens in a new tab)

  11. Enantioselective nucleophile-catalyzed cycloadditions

    … of an asymmetric nucleophile-catalyzed [2+2] cycloaddition of ketenes with aldehydes. This is the first report of a catalytic enantioselective synthesis of trisubstituted [beta]-lactones. Two enantioselective phosphine-catalyzed [3+2] cycloadditions of allenoates are detailed in Chapter 2. A …

    mit Repository record for Enantioselective nucleophile-catalyzed cycloadditions (opens in a new tab)

  12. Part I. Total Synthesis and Structural Revision of (±)-Tricholomalides A and B. Part II. Synthetic Studies towards (+)-Cortistatin A

    … annulation, followed by a ketene-olefin [2+2] cycloaddition to introduce the lactone ring. Then a Grignard-type reaction appended the isopropenyl moiety, and the synthesis of tricholomalides A and B was achieved. During the course of synthesis, the structures of tricholomalides A and B were …

    columbia-diss Repository record for Part I. Total Synthesis and Structural Revision of (±)-Tricholomalides A and B. Part II. Synthetic Studies towards (+)-Cortistatin A (opens in a new tab)

  13. Synthesis of pyridines via [4 + 2] cycloadditions of vinylallenes with azadienophiles

    … substituted pyridines that involve [4 + 2] cycloadditions of vinylallenes with azadienophiles. Part II of this thesis describes a unimolecular, formal [2 + 2 + 2] cycloaddition strategy for the synthesis of tricyclic pyridines based on intramolecular propargylic ene/imino Diels-Alder …

    mit Repository record for Synthesis of pyridines via [4 + 2] cycloadditions of vinylallenes with azadienophiles (opens in a new tab)

  14. Synthetic studies towards total synthesis of bielschowskysin

    … butenolide was prepared in 13 steps and [2+2] cycloaddition was carried out under the UV lamps to form the tricyclic core of bielschowskysin. After making the tricyclic core, retrosynthetic analysis of key intermediate leads to left and right fragment. Left fragment, seleno-lactone was prepared …

    nus Repository record for Synthetic studies towards total synthesis of bielschowskysin (opens in a new tab)

  15. Novel Photochemical Methodologies for Diversity Oriented Synthesis and Screening of Combinatorial Libraries

    … are capable of photoinduced alkene-arene [2+2] cycloaddition producing different dienes, which can either dimerize or be introduced into a double-tandem [4<sub>π</sub>+2<sub>π</sub>]·[2<sub>π</sub>+2<sub>π</sub>]·[4<sub>π</sub>+2<sub>π</sub>]·[2<sub>π</sub>+2<sub>π</sub>] synthetic sequence, …

    denver Repository record for Novel Photochemical Methodologies for Diversity Oriented Synthesis and Screening of Combinatorial Libraries (opens in a new tab)

  16. New routes to enantioenriched substances through small organic molecules

    … and bicyclo[3.2.0]hept-3-en-6-ones through a cycloaddition strategy is reported. The fundamental step is a [2+2]-cycloaddition of an enantiopure amide derived from the reaction between a set of acids and an oxazolidinone as the chiral auxiliary. The inter- and intramolecular cycloaddition of …

    bologna Repository record for New routes to enantioenriched substances through small organic molecules (opens in a new tab)

  17. Entwicklung photosensitiver Polymernetzwerke mit Formgedächtniseigenschaften

    … is controlled by the light-induced [2+2]-cycloaddition of cinnamates. The synthesis of amorphous covalently linked polyacrylate networks is reported. Acrylate monomers containing cinnamic acid groups lead to photoreactive groups in polymer side- chains. Those monomers are prepared by …

    aachen Repository record for Entwicklung photosensitiver Polymernetzwerke mit Formgedächtniseigenschaften (opens in a new tab)

  18. Synthesis of derivatives of 4H-cyclopenta[ def]phenanthren-4-one and development of synthetic strategies for the polycyclic aromatic hydrocarbons with carbon frameworks represented on the surface of C60

    … then afforded the formal [4+2] Diels-Alder cycloaddition adduct 60, which in turn underwent tautomerization to give 61. Reduction with tri-n-butyltin hydride then gave the ketal 62 in 46% overall yield from 56a. Hydrolysis of the ketal 62 gave the ketone 51 in 97% yield.;Another derivative …

    wvu Repository record for Synthesis of derivatives of 4H-cyclopenta[ def]phenanthren-4-one and development of synthetic strategies for the polycyclic aromatic hydrocarbons with carbon frameworks represented on the surface of C60 (opens in a new tab)

  19. Pericyclic reactions in organic synthesis

    … describes a formal, metal-free, [2 + 2 + 2] cycloaddition strategy based on a cascade of two pericyclic processes. An intramolecular propargylic ene reaction of a 1,6-diyne is used to generate a vinylallene, which then reacts in an inter- or intramolecular Diels-Alder reaction with an alkenyl …

    mit Repository record for Pericyclic reactions in organic synthesis (opens in a new tab)

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