Nate W. J. Ang

ORCID: 0000-0003-3977-2676
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About
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Research Areas
  • Radical Photochemical Reactions
  • Catalytic C–H Functionalization Methods
  • Carbon dioxide utilization in catalysis
  • Sulfur-Based Synthesis Techniques
  • Oxidative Organic Chemistry Reactions
  • CO2 Reduction Techniques and Catalysts
  • Asymmetric Hydrogenation and Catalysis
  • Catalytic Cross-Coupling Reactions
  • Chemical Synthesis and Analysis
  • Organoboron and organosilicon chemistry
  • X-ray Diffraction in Crystallography
  • Green IT and Sustainability
  • Crystallization and Solubility Studies

University of Göttingen
2018-2021

University of Edinburgh
2017

Abstract The chemical use of CO 2 as an inexpensive, nontoxic C1 synthon is utmost topical interest in the context carbon capture and utilization (CCU). We present merger cobalt catalysis electrochemical synthesis for mild catalytic carboxylations allylic chlorides with . Styrylacetic acid derivatives were obtained moderate to good yields functional group tolerance. thus‐obtained products are useful versatile synthons γ‐arylbutyrolactones. Cyclic voltammetry operando kinetic analysis...

10.1002/anie.202003218 article EN cc-by-nc Angewandte Chemie International Edition 2020-04-24

Versatile cobalt catalysis enabled electrochemical C–H activation with allenes. Thus, allene annulations were accomplished in terms of C–H/N–H functionalizations excellent levels chemoselectivity, site selectivity, and regioselectivity under exceedingly mild conditions. Detailed mechanistic studies conducted, including reactions isotopically labeled compounds, kinetic investigations, in-operando infrared spectroscopic studies. Further, computational supportive a non-rate-determining cleavage...

10.1021/acscatal.8b03066 article EN ACS Catalysis 2018-08-15

Simple, commercially available borane adducts, H3B·THF and H3B·SMe2, have been used to catalyse the hydroboration of alkynes alkenes with pinacolborane give alkenyl alkyl boronic esters, respectively. Alkynes terminal underwent highly regioselective linear ester products. Good functional group tolerance was observed for substrates bearing ester, amine, ether halide substituents. This catalytic process shows comparable reactivity transition-metal-catalysed protocols.

10.1055/s-0036-1591719 article EN Synthesis 2017-11-20

Sulfur-containing molecules are of utmost topical importance towards the effective development pharmaceuticals and functional materials. Herein, we present an efficient mild electrochemical thiolation by cross-electrophile coupling alkyl bromides with functionalized bench-stable thiosulfonates to access sulfides excellent efficacy broad group tolerance. Cyclic voltammetry potentiostatic analysis were performed elucidate mechanistic insights into this electrocatalytic reaction.

10.1002/chem.202005449 article EN cc-by-nc Chemistry - A European Journal 2020-12-28

Abstract Die chemische Verwendung von CO 2 als kostengünstiges und ungiftiges C1‐Synthon ist bedeutendem Interesse für den Kohlenstoffhaushalt in Bezug auf Einfang (CCU). Wir präsentieren die Fusion Cobalt‐Katalyse elektrochemischer Synthese milde katalytische Carboxylierung Allylchloriden mit . Styrylessigsäure‐Derivate wurden mäßigen bis guten Ausbeuten guter Toleranz gegenüber funktionellen Gruppen erhalten. so erhaltenen Produkte sind vielseitige Synthons γ‐Arylbutyrolactone nützlich....

10.1002/ange.202003218 article DE cc-by-nc Angewandte Chemie 2020-04-24
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