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Coordination Compounds of Some Polydentate Cyclic Amines: I. Tridentate Amines. II. Bidentate Amines

Middleton, Errol BathurstUniversity of Illinois at Urbana-Champaign1939

uiuc Repository record for Coordination Compounds of Some Polydentate Cyclic Amines: I. Tridentate Amines. II. Bidentate Amines (opens in a new tab)

New chiral molybdenum metathesis catalysts : application to the enantioselective preparation of cyclic amines

Dolman, Sarah Jennifer, 1977-Massachusetts Institute of Technology2004

… desymmetrization of unsaturated prochiral amines to afford tetrahydropyridines (2.68a-e). The selectivity of this transformation was sensitive to the olefin substitution pattern of the prochiral amine. However, this novel method was also applicable for the formation seven-(2.84), and …

mit Repository record for New chiral molybdenum metathesis catalysts : application to the enantioselective preparation of cyclic amines (opens in a new tab)

I. Study of the internal Mannich reaction. II. Study of the Clemmensen reduction of five- and seven-membered cyclic amines containing the ketone function

Barthel, Eric, Jr.University of Illinois Urbana-Champaign1950

uiuc Repository record for I. Study of the internal Mannich reaction. II. Study of the Clemmensen reduction of five- and seven-membered cyclic amines containing the ketone function (opens in a new tab)

I. Reactions of 4-quinazolone with compounds containing the amine function. II. Study of the Clemmensen reduction of six-membered cyclic amines containing the ketone function

Ruyle, William VanceUniversity of Illinois at Urbana-Champaign1949

uiuc Repository record for I. Reactions of 4-quinazolone with compounds containing the amine function. II. Study of the Clemmensen reduction of six-membered cyclic amines containing the ketone function (opens in a new tab)

Palladium-Catalysed Functionalisation of Csp3–H Bonds Directed by Aliphatic Amines

Buettner, CorneliaUniversity of Cambridge2020

… on medicinally-relevant aliphatic amines are valuable in the diversification of molecules designed as pharmaceutical agents. This thesis describes two Csp3–H functionalisation reactions, using native amines (secondary and tertiary) to direct C–H activation. Chapter 2 describes a …

cambridge Repository record for Palladium-Catalysed Functionalisation of Csp3–H Bonds Directed by Aliphatic Amines (opens in a new tab)

1,3-Aminoalkohole als Bausteine in der asymmetrischen Synthese von Azetidinen, Azetidincarbonsäuren und Piperidin-3-olen

Gries, JörgPublikationsserver der RWTH Aachen University2005

Four-membered cyclic amines – the azetidines – are an original class of compounds with limited occurrence in nature. Nevertheless enantiopure azetidines and in particular derivatives of the azetidine-2-carboxylic acid are used in medicine, crop protection and asymmetric catalysis. Despite these …

aachen Repository record for 1,3-Aminoalkohole als Bausteine in der asymmetrischen Synthese von Azetidinen, Azetidincarbonsäuren und Piperidin-3-olen (opens in a new tab)

Palladium-mediated C–H Functionalization of Aliphatic Amines via High Valent Palladium(IV) Intermediates

Whitehurst, WilliamUniversity of Cambridge2020

… C–H functionalization of unprotected aliphatic amines, in which the amine nitrogen coordinates to the Pd centre to promote cyclometalation to the key palladacycle intermediate. Specifically, research focused on the design and optimization of novel oxidants that would provide mild and general …

cambridge Repository record for Palladium-mediated C–H Functionalization of Aliphatic Amines via High Valent Palladium(IV) Intermediates (opens in a new tab)

The development of directing group enabled hydroamination strategies to access to 1,2-, 1,3-, and 1,4- diamines with high levels of regio-, chemo-, and stereoselectivity

Vanable, Evan PatrickUniversity of Illinois at Urbana-Champaign2019

… reaction of olefins, as olefins and amines are both readily accessible. This reaction has the potential to be entirely atom-economical, as well as modular. Another advantage, and concomitant challenge, that comes with this strategy, is the ability to form multiple isomers: there are …

uiuc Repository record for The development of directing group enabled hydroamination strategies to access to 1,2-, 1,3-, and 1,4- diamines with high levels of regio-, chemo-, and stereoselectivity (opens in a new tab)

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)

Synthesis and Characterization of Poly(2-Ethyl-2-Oxazoline) Functional Prepolymers and Block Copolymers

Celebi, OguzhanVirginia Tech2014

… all cases, termination reactions with aliphatic cyclic amines were quantitative. Mono- and diamine functional PEtOx oligomers with controlled molecular weight and excellent end-group functionality may be used as prepolymers for incorporation into multiblock and graft copolymer and crosslinked …

vt Repository record for Synthesis and Characterization of Poly(2-Ethyl-2-Oxazoline) Functional Prepolymers and Block Copolymers (opens in a new tab)

Development of Deactivation-Resistant Catalysts for Pd-Catalyzed C–N Cross-Coupling Reactions

Reichert, Elaine C.Massachusetts Institute of Technology2023

… reactions between a variety of primary amines and aryl halides, was developed; in many cases, these reactions can be carried out at room temperature. The reaction development was guided by the idea that the productivity of catalysts employing BrettPhos-like ligands is limited by their …

mit Repository record for Development of Deactivation-Resistant Catalysts for Pd-Catalyzed C–N Cross-Coupling Reactions (opens in a new tab)