Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Matthew B. Prater"'
Autor:
Hui Chen, Tianhua Tang, Christian A. Malapit, Yoo Seok Lee, Matthew B. Prater, N. Samali Weliwatte, Shelley D. Minteer
Publikováno v:
Journal of the American Chemical Society. 144:4047-4056
Petroleum hydrocarbons are our major energy source and an important feedstock for the chemical industry. With the exception of combustion, the deep conversion of chemically inert hydrocarbons to more valuable chemicals is of considerable interest. Ho
Autor:
Skylar Blank, Christian A. Malapit, Matthew B. Prater, Min Li, Jaime R. Cabrera-Pardo, Timothy Patrick McFadden, Shelley D. Minteer, Tammy Dung Pham
Publikováno v:
Chem Rev
Synthetic organic electrosynthesis has grown in the past few decades by achieving many valuable transformations for synthetic chemists. Although electrocatalysis has been popular for improving selectivity and efficiency in a wide variety of energy-re
Critical role of structural order in bipolar redox-active molecules for organic redox flow batteries
Autor:
Julia Case, Zayn Rhodes, Ilya A. Shkrob, Shelley D. Minteer, Ryan T. VanderLinden, Rajeev S. Assary, Min Li, Matthew B. Prater, Garvit Agarwal
Publikováno v:
Journal of Materials Chemistry A. 9:23563-23573
Bipolar redox-active molecules (BRMs) have been suggested as a means to address crossover related issues in all-organic redox flow batteries (RFBs). In such species, electron donors (anolytes) and electron acceptors (catholytes) are linked by a chain
Autor:
Hui Chen, Shelley D. Minteer, Mengwei Yuan, Matthew B. Prater, Fangyuan Dong, Christian A. Malapit, Min Li, Koun Lim
Publikováno v:
Journal of the American Chemical Society. 142:8374-8382
Two obstacles limit the application of oxidoreductase-based asymmetric synthesis. One is the consumption of high stoichiometric amounts of reduced cofactor. The other is the low solubility of organic substrates, intermediates, and products in the aqu
Autor:
John E. Matthiesen, Min Li, Jack Lee, Kevin J. Klunder, Matthew B. Prater, Shelley D. Minteer, Emmy Blumenthal
Publikováno v:
ACS Sustainable Chemistry & Engineering. 8:4489-4498
N-Oxyl reagents, particularly 2,2,6,6-tetramethylpiperidine 1-oxyl (TEMPO), have been extensively used for alcohol oxidations. While TEMPO-mediated oxidations are kinetically and thermodynamically ...
Bioelectrocatalytic Conversion from N2 to Chiral Amino Acids in a H2/α-Keto Acid Enzymatic Fuel Cell
Publikováno v:
Journal of the American Chemical Society. 142:4028-4036
Enzymatic electrosynthesis is a promising approach to produce useful chemicals with the requirement of external electrical energy input. Enzymatic fuel cells (EFCs) are devices to convert chemical ...
Autor:
Puneet Kumar, Janis Louie, Judah L. Evangelista, Philipp M. Rutz, Ashish Thakur, Jacob M. Cowley, Matthew B. Prater, Jonas Renner, Ryan M. Stolley
Publikováno v:
Organic Letters. 22:924-928
A Ni-catalyzed (4 + 2) cycloaddition of alkynes and azetidinones toward piperidinones was used as key reaction in the enantioselective synthesis of naturally occurring indolizidine alkaloids. The reaction benefits from the use of an easily accessible
Autor:
Matthew B. Prater, Matthew S. Sigman
Publikováno v:
Isr J Chem
Herein we report a transformation that generates an array of enantiomerically enriched, alkyl allyl ethers. Cyclic, acyclic, and heteroatom-bearing alkenyl triflates undergo an enantioselective, palladium-catalyzed C–C bond formation with diverse a
Publikováno v:
Journal of the American Chemical Society. 142(8)
Enzymatic electrosynthesis is a promising approach to produce useful chemicals with the requirement of external electrical energy input. Enzymatic fuel cells (EFCs) are devices to convert chemical energy to electrical energy via the oxidation of fuel
Publikováno v:
Journal of the American Chemical Society. 140:5895-5898
This report details a palladium-catalyzed process to access highly functionalized, optically active allylic aryl ethers. A number of electron-deficient alkenyl triflates underwent enantioselective and site-selective coupling with acyclic aryl enol et