Global ETD Search

Search theses and dissertations gathered from participating repositories worldwide. Every result links back to the library that holds it. No account is needed.

Results

Showing 1 to 5 of 5 for “"carboamination"”.

  1. Total synthesis enabled by nickel-catalyzed transformations: Dearomative carboamination and methylenecyclopropane annulation

    … a novel nickel-catalyzed asymmetric dearomative carboamination reaction. This strategy relies on the ability of N-methyl-1,2,4-triazoline-3,5-dione (MTAD) to undergo a [4+2] cycloaddition with benzene to form an intermediary cycloadduct that can then be subjected to a transition metal and …

    uiuc Repository record for Total synthesis enabled by nickel-catalyzed transformations: Dearomative carboamination and methylenecyclopropane annulation (opens in a new tab)

  2. I. Palladium-catalyzed anti-Markovnikov oxidative amination of olefins II. Catalytic deracemization of axially chiral diols III. Three component carboamination of electron deficient alkenes

    … we have developed a copper-catalyzed 3-component carboamination reaction. This transformation converts alkenes, aryl amines, and alkyl halides into densely functionalized lactams. The use of acrylate alkenes is a notable step forward in the area of radical carboamination, as previous work has …

    uiuc Repository record for I. Palladium-catalyzed anti-Markovnikov oxidative amination of olefins II. Catalytic deracemization of axially chiral diols III. Three component carboamination of electron deficient alkenes (opens in a new tab)

  3. Development of three-component alkene and 1,3-diene carbofunctionalization reactions

    … we have developed a three-component alkene carboamination reaction. This system offers access to complex amine products from simple starting materials and proceeds under mild reaction conditions. Critically, this transformation combines disconnected carbon, nitrogen, and alkene moieties as …

    uiuc Repository record for Development of three-component alkene and 1,3-diene carbofunctionalization reactions (opens in a new tab)

  4. Advances in synthetic methodology: Dearomative aminofunctionalization of arenes and high-throughput reaction discovery

    Submission original under an indefinite embargo labeled 'Open Access'. The submission was exported from vireo on 2025-03-28 without embargo terms

    uiuc Repository record for Advances in synthetic methodology: Dearomative aminofunctionalization of arenes and high-throughput reaction discovery (opens in a new tab)