Results 121 to 130 of about 52,626 (269)

FLP Mediated Conversion of Difluorobenzylalkynes to Fluoroallenyl Oniums via an SN1’ Pathway

Chemistry – A European Journal, EarlyView.
Frustrated Lewis pair (FLP) selective C‒F activation of difluorobenzylalkynes allows the formation of fluoroallenic oniums via an SN1’ substitution pathway. The fluoroallenic onium salts are synthetic precursors that allow subsequent functionalization at allenic and onium positions.
Max Coles, Tianhong Wang, Rubi McLennan, Long Kit Kwan, Bivas Mondal, Chakyu Richard Chan, Rowan D. Young   +6 more
wiley   +1 more source

Push-pull systems based on pyridinium betaines.

, 2012
Byla provedena literarni rešerše mapujici využiti a synteticke postupy vedouci k push-pull systemům na bazi pyridinium betainů. Využiti těchto latek spočiva předevšim v jejich NLO vlastnostech.
Miklík, David
core   +1 more source

Stereoretentive Nucleophilic Aromatic Substitution Accesses Atropisomeric 4‐Amino‐N‐Arylquinolinium Salts

Chemistry – A European Journal, EarlyView.
Quinolin‐4‐ones were converted to chloroquinolinium salts, allowing formation of axially chiral aminoquinolinium salts via an enantioretentive SNAr reaction with a variety of amine nucleophiles. The salts have a high rotational barrier, with a racemization half‐life of ∼1000s of years.
Darren Holmes, Nia Foster, Saima Ansari, Paul Kavanagh, Paul Dingwall, Peter C. Knipe   +5 more
wiley   +1 more source

Bis(4,4′-bipyridin-1-ium) cis-bis(1,2-dicyano-2-sulfidoethene-1-sulfinato-κ2S,S′)platinate(2−)

IUCrData
Crystals of the sulfinate-containing platinate salt, (C10H9N2)2[Pt(C4N2O2S2)2], were obtained from a solution of [Pt(4,4′-bpy)2(mnt)] after a long period with minimal light (4,4′-bpy is 4,4′-bipyridine and mnt is maleonitriledithiolate). In the crystals,
Claire E. Welton, Eric W. Reinheimer, Bradley W. Smucker   +2 more
doaj   +1 more source

Nitrooxylation in Organic Synthesis: From Classical Nitrate Ester Formation to Modern Catalytic Strategies

Chemistry – A European Journal, EarlyView.
Nitrooxylation—the installation of nitrate esters (–ONO2) has evolved from classical mixed‐acid protocols to catalytic and mechano‐, flow‐, photo‐, and electrochemical strategies. This review delineates ionic and radical manifolds for C–ONO2 bond formation, emphasizing mechanistic control, selected substrate scope, and selectivity.
Jayanta Dey, Dmitry Katayev
wiley   +1 more source

Pyridinium-based fluorosulfonamide reagents enabled photoredox catalyzed radical fluorosulfonamidation [PDF]

Sulfamoyl fluorides, as a crucial building block of SuFEx, have garnered extensive research interest due to their applications in chemical biology, materials science, and drug discovery. Recently, considerable research has been dedicated to the synthesis
Chao, Sun, Weigang, Zhang, Jing, Liu, Xian, Zhang, Heyin, Li, Zhenlei, Zou, Zhen, Wang, Yi, Pan, Mengjun, Huang, Yifan, Li, Yi, Wang   +10 more
core   +2 more sources

π‐Extended Salphen Scaffolds Enable CO2 Electroreduction and Singlet Oxygen Generation

Chemistry – A European Journal, EarlyView.
New family of π‐extended salen ligands bearing phenylene bridge and tunable phenyl‐based substituents, and their corresponding boron difluoride complexes. Thanks to the extended π‐delocalization over the molecule, the ligands themselves show promising results in electrochemical CO2 reduction to CO, while the complexes act as efficient photosensitizers ...
Vincenzo Langellotti, André Korzun, Morgan J. McKee, Massimo Melchiorre, Taegeun Jo, J. Felipe Estrada‐Ruiz, Gregor Schnakenburg, Stefano Crespi, Francesco Ruffo, Nikolay Kornienko, Alessandro Bismuto   +10 more
wiley   +1 more source

Hybrid Macrocyclic Peptides — Synthetic Strategies to Diversify and Cyclize Peptide Libraries in Phage Display Selections

Chemistry – A European Journal, EarlyView.
Hybrid macrocyclic peptides unite genetically encoded peptide libraries with the structural complexity of synthetic small molecules. This Review critically analyzes phage‐compatible cyclization and diversification chemistries, highlights emerging opportunities beyond traditional cysteine‐based approaches, and outlines how future advances may enable the
Titia Rixt Oppewal, Clemens Mayer
wiley   +1 more source

Investigating the chemistry of pyridinium ylides [PDF]

, 2018
This thesis describes investigation into catalytic formation of pyridinium ylides from diazo compounds and their subsequent reactivity. In particular, cycloaddition reactions with electrophilic alkenes are performed to generate tetrahydroindolizines that
Abdullah, Rasha Azzam
core  

Expanding the Scope of Indium in Frustrated Lewis Pair Chemistry

Chemistry – A European Journal, EarlyView.
All good things come in threes: The pyridine‐“protected” FLP tBu2InCH2PtBu2·Py shows three different kinds of reactivity: Besides “typical” FLP activity, it prefers formation of the “soft” isomers for substrates with multiple sites for FLP attack, but reacts with SO2 as a “masked” In/C FLP by insertion into the In─C bond.
Daniel N. Heuer, Jan‐Hendrik Lamm, Beate Neumann, Andreas Mix, Yury V. Vishnevskiy, Norbert W. Mitzel   +5 more
wiley   +1 more source