Effects of the Backbone's Structures on the Curing Behaviors and Properties of Phthalonitrile Containing Benzoxazine Rings. [PDF]
Xu M, Zhang J, Li B, Fan Z, He L.
europepmc +1 more source
Study on the Curing Behaviors of Benzoxazine Nitrile-Based Resin Featuring Fluorene Structures and the Excellent Properties of Their Glass Fiber-Reinforced Laminates. [PDF]
Xu M, He L, Zhang J, Fan Z, Li B.
europepmc +1 more source
An Update: Enzymatic Synthesis for Industrial Applications
Biocatalysis has become a sustainable and cost‐competitive alternative to established chemical synthesis, enabling the enzyme‐based production of not only commodity chemicals but (non‐natural) amino acids, (rare) sugars, as well as synthetic nucleotides.
Thomas Bayer+4 more
wiley +1 more source
Cycloaddition reaction of NaN<sub>3</sub> with nitriles toward the synthesis of tetrazoles catalyzed by a copper complex on boehmite nanoparticles. [PDF]
Jabbari A+3 more
europepmc +1 more source
Poly(arylene ether nitrile) Based Dielectrics with High Energy Storage Properties: A Review. [PDF]
Liu Y+9 more
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The Puzzle of the Regioselectivity and Molecular Mechanism of the (3+2) Cycloaddition Reaction Between E-2-(Trimethylsilyl)-1-Nitroethene and Arylonitrile N-Oxides: Molecular Electron Density Theory (MEDT) Quantumchemical Study. [PDF]
Sadowski M, Dresler E, Jasiński R.
europepmc +1 more source
Reactivity of Pnictaalumenes towards 1,3‐Dipole Molecules
Alkynes undergo 1,3‐dipolar cyclisation reactions with organic azides giving 1,2,3‐triazoles. Pnictaalumenes RPn=AlRˈ are the isoelectronic congeners of alkynes, hence a similar reactivity towards 1,3‐dipole molecules is expected. Herein, we report the reactions of DippTerPn=AlCp* (DippTer = 2,6‑(2,6‐iPr2C6H3)‐C6H3, Cp* = [Me5C5]−, Pn = P, As) towards ...
Tim Wellnitz+7 more
wiley +1 more source
Engineering the solid electrolyte interphase for enhancing high-rate cycling and temperature adaptability of lithium-ion batteries. [PDF]
Wang Z+8 more
europepmc +1 more source
Aldoxime dehydratases: production, immobilization, and use in multistep processes. [PDF]
Martínková L+5 more
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Redirecting the Peptide Cleavage Causes Protease Inactivation
Cysteine and serine proteases cleave peptides through covalent catalysis by generating a transient adduct with the N‐terminal part of the substrate after releasing its C‐terminal part. We demonstrate the unique redirection of this event leading to strong enzyme inactivation.
Michael Gütschow+20 more
wiley +1 more source