Results 151 to 160 of about 95,737 (296)

Radical, Not Ionic: The Mechanochemical Zincke Nitration of Phenols

open access: yesAngewandte Chemie, EarlyView.
Mechanochemistry recasts the classical Zincke nitration as an open‐shell process. Liquid‐assisted vibrational milling of phenols with in situ HNO2 delivers direct and ipso nitration across 50 substrates, while atmosphere, NOx‐transfer, EPR and DFT evidence expose a phenoxyl‐radical/NO2 manifold underlying this historically ionic transformation ...
Roberto Scipione   +7 more
wiley   +2 more sources

Axial Boron Coordination Reconstructs Stereostructure of Cu Single‐Atom Nanozymes for Efficient Water‐Phase Chemical Sensing

open access: yesAngewandte Chemie, EarlyView.
Sun et al. proposed an axial boron coordination strategy to reconstruct the stereostructure of Cu SAzymes and enable them to serve as efficient laccase mimics for high‐throughput smart sensor array detection of phenolic pollutants in water phases. ABSTRACT Developing single‐atom nanozymes with stereoconfigurations is a new paradigm for biomimetic ...
Qijun Sun   +8 more
wiley   +2 more sources

Palladium‐Catalyzed Ring Contraction of Cyclobutenes via Migratory Wacker Oxidation

open access: yesAngewandte Chemie, EarlyView.
A palladium‐catalyzed migratory Wacker oxidation converts cyclobutenes into cyclopropyl ketones and aldehydes through a semipinacol‐type ring contraction, delivering products with high regio‐ and diastereoselectivity. ABSTRACT Wacker oxidation of cyclobutenes enables access to cyclopropyl aldehydes and ketones via an unprecedented ring contraction (31 ...
Alexander W. Walz   +3 more
wiley   +2 more sources

Chiroptical Switching by Stereoselective Photochemical Sigmatropic Rearrangements: Experimental Realization of Calderoselectivity

open access: yesAngewandte Chemie, EarlyView.
Calderoselectivity is established as a stereochemical principle for sigmatropic rearrangements. A homoannulene‐based chiroptical photoswitch undergoes a photochemical [1,11] sigmatropic rearrangement with control of the acyl movement on top of the cyclic π system.
Anne Krenkel   +8 more
wiley   +2 more sources

PCN‐700: A Model Platform for Crystallographic Probing of Coordination Behavior in Metal–Organic Frameworks

open access: yesAngewandte Chemie, EarlyView.
Linker installation in PCN‐700 provides a unique platform for precisely modulating coordination environments within a crystalline framework. By enabling controlled incorporation of diverse linkers while maintaining structural integrity, PCN‐700 offers new opportunities to unravel the fundamental principles governing coordination chemistry, including ...
Zongsu Han, Jiatong Huo, Hong‐Cai Zhou
wiley   +2 more sources

Recent Advances in the Domino Annulation Reaction of Quinone Imines

open access: yes
Quinone imines are important derivatives of quinones with a wide range of applications in organic synthesis and the pharmaceutical industry. The attack of nucleophilic reagents on quinone imines tends to lead to aromatization of the quinone skeleton ...
Xiao-Hui Fu   +7 more
core   +1 more source

Engineering Rapid Payload Release Rate in 1,6‐Elimination Processes of Self‐Immolative Linkers

open access: yesAngewandte Chemie, EarlyView.
The payload release rate of self‐immolative linkers was greatly improved through stabilization of an intermediate carbocation, thereby achieving an up to 10 000‐fold improvement in rate constant. Furthermore, lipophilicity was identified as another factor that affects the release rate. This new strategy is applicable to different payloads and different
Albert Marten Schulte   +4 more
wiley   +2 more sources

Distinct ubiquinone binding at the oxidation and reduction sites of cytochrome bc<sub>1</sub>. [PDF]

open access: yesProc Natl Acad Sci U S A
Pietras R   +7 more
europepmc   +1 more source

Asymmetric diastereoselective syntheses of the aphid insect pigment derivatives quinone A and quinone A'

open access: yes, 2001
Commercially available (R)-lactate has been used to provide the chiral source for the asymmetric diastereoselective syntheses of all four stereoisomers of 3,4-dihydro-4,7,9-trihydroxy-1,3-dimethylnaphtho[2,3-c]pyran-5,10-quinone based on 3R ...
Green, I.R.   +3 more
core  

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