Global ETD Search

I. The Clemmensen reduction-rearrangement of phenyl-substituted α-aminoketones. II. The electrolytic reduction of tricyclic α-aminoketones

Fuller, GlennUniversity of Illinois at Urbana-Champaign1954

uiuc Repository record for I. The Clemmensen reduction-rearrangement of phenyl-substituted α-aminoketones. II. The electrolytic reduction of tricyclic α-aminoketones (opens in a new tab)

The Clemmensen Reduction cum Rearrangement of Alpha-Aminoketones

Pines, Seemon HaydenUniversity of Illinois at Urbana-Champaign1951

uiuc Repository record for The Clemmensen Reduction cum Rearrangement of Alpha-Aminoketones (opens in a new tab)

The Behavior of α-Thiaketones and α-Aminoketones under Conditions of the Clemmensen Reduction and Electrolytic Reduction

Figueras, JohnUniversity of Illinois at Urbana-Champaign1952

uiuc Repository record for The Behavior of α-Thiaketones and α-Aminoketones under Conditions of the Clemmensen Reduction and Electrolytic Reduction (opens in a new tab)

A Promiscuous Path to Novel Guanidines: Arginine-Modifying Enzymes as Key Synthetic Players

Fakhry, Ayman A.A.University of Bradford2026

… 2-aminoimidazole derivatives. A wide range of α-aminoketones of arginine, arginine derivatives, and analogues were prepared either synthetically or by leveraging the promiscuous C-C bond forming capacity of an engineered SxtA-AOS variant. These α-aminoketones serve as substrates for SxtG1-3, in …

bradford Repository record for A Promiscuous Path to Novel Guanidines: Arginine-Modifying Enzymes as Key Synthetic Players (opens in a new tab)

I. 1,2-Dimethylene- and 1,2-Dioxo-cycloalkanes: Structure, Spectra, and Relation to Their Open-Chain Analogs. II. Medium Rings via Electrolytic Reduction of Bicyclic α-Aminoketones

Mottus, Edward HugoUniversity of Illinois at Urbana-Champaign1953

uiuc Repository record for I. 1,2-Dimethylene- and 1,2-Dioxo-cycloalkanes: Structure, Spectra, and Relation to Their Open-Chain Analogs. II. Medium Rings via Electrolytic Reduction of Bicyclic α-Aminoketones (opens in a new tab)

Organokatalytische Synthesen biologisch aktiver Naturstoffe : Totalsynthesen von Amaminol A und B und (+)-Mitsugashiwalacton sowie Synthesen 2,6-disubstituierter Tetrahydropyranen

Jacobs, Wiebke CordulaPublikationsserver der RWTH Aachen University2009

… Horner-Wadsworth-Emmons reaction generated N-Boc-aminoketones. A Raney® nickel reduction of the conjugated double bond and, in the case of amaminol A, a syn-selective and, in the case of amaminol B, an anti-selective reduction resulted in N-Boc-amaminole A und B with very attractive yields and …

aachen Repository record for Organokatalytische Synthesen biologisch aktiver Naturstoffe : Totalsynthesen von Amaminol A und B und (+)-Mitsugashiwalacton sowie Synthesen 2,6-disubstituierter Tetrahydropyranen (opens in a new tab)

I. Development of three-component alkene carboamination reactions II. Palladium-catalyzed anti-Markovnikov oxidative amination of alkenes III. Chloroform as a carbon monoxide precursor: in or ex situ generation of co for pd-catalyzed carbonylations IV. Hydroalkylation of alkenes via photoredox catalysis

Gockel, Samuel NoahUniversity of Illinois at Urbana-Champaign2019

… and later leveraged for the formation of aminoketones from homoallylic alcohols. The carbonylation of organic halides utilizing chloroform as the carbonyl source has also been developed. This new carbonylation method allows for the amino-, thio-, and alkoxycarbonylation of aryl and vinyl …

uiuc Repository record for I. Development of three-component alkene carboamination reactions II. Palladium-catalyzed anti-Markovnikov oxidative amination of alkenes III. Chloroform as a carbon monoxide precursor: in or ex situ generation of co for pd-catalyzed carbonylations IV. Hydroalkylation of alkenes via photoredox catalysis (opens in a new tab)