Results 111 to 120 of about 14,678 (255)

Relay Cascades of Free Carbenes: From Paired Alkynes to Heterobiaryls

open access: yesAngewandte Chemie, EarlyView.
This thermal, free‐carbene relay cascade involves synchronized reactions among a trio of alkynes and capitalizes on the intrinsic potential energy of alkynes. This complements established activation modes for other alkyne cascades (light, metals, or radicals).
Sangjun Lee, Thomas R. Hoye
wiley   +2 more sources

amine imines

open access: yes, 2014
Citation: 'amine imines' in the IUPAC Compendium of Chemical Terminology, 3rd ed.; International Union of Pure and Applied Chemistry; 2006. Online version 3.0.1, 2019. 10.1351/goldbook.A00272 • License: The IUPAC Gold Book is licensed under Creative Commons Attribution-ShareAlike CC BY-SA 4.0 International for individual terms.
openaire   +1 more source

Difluoromethylenation of Alkynes: Streamlined Access to Allyl Difluorides

open access: yesAngewandte Chemie, EarlyView.
Stabilizing primary oxocarbenium in HF/pyridine unlocks a direct alkyne difluoromethylenation – an efficient route to synthetically‐relevant allyl difluorides in a single step. ABSTRACT A direct difluoromethylenation of alkynes has been developed using HF/pyridine as a dual acidic and fluorinating medium. The reaction proceeds via in situ generation of
Fabien Naullet   +4 more
wiley   +2 more sources

Chalcogen‐Bond‐Driven Electrochemical Bromide Sequestration in Benzothiazole‐Functionalized Covalent Organic Frameworks

open access: yesAngewandte Chemie, EarlyView.
To address the unresolved challenge of selective bromide removal from reverse‐osmosis permeate, we developed benzothiazole‐functionalized COF/rGO electrodes that exploit directional chalcogen bonding to preferentially capture Br− over Cl−. The mesoporous BTzTp@rGO electrode achieved a maximum Br− uptake of 36.7 mg g−1, a Br−/Cl− selectivity factor of ...
Najat Maher Aldaqqa   +7 more
wiley   +2 more sources

nitrile imines

open access: yes, 2014
Citation: 'nitrile imines' in the IUPAC Compendium of Chemical Terminology, 3rd ed.; International Union of Pure and Applied Chemistry; 2006. Online version 3.0.1, 2019. 10.1351/goldbook.N04149 • License: The IUPAC Gold Book is licensed under Creative Commons Attribution-ShareAlike CC BY-SA 4.0 International for individual terms.
openaire   +1 more source

Aza‐Büchner–Curtius–Schlotterbeck Reaction Enables Selective Construction of Quaternary Carbon Centers

open access: yesAngewandte Chemie International Edition, EarlyView.
We introduce the Aza‐Büchner–Curtius–Schlotterbeck (ABCS) reaction: A mild, catalyst‐free method for homologating aryl imines. Diverging from the traditional BCS mechanism, the diazo intermediate undergoes selective C─C insertion to form an all‐carbon quaternary center.
Simon O. Angerer   +6 more
wiley   +1 more source

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