Results 111 to 120 of about 13,633 (275)

Photocatalytic Vanadium‐Mediated Amination of Benzene With Hydroxylamine

open access: yesChemistry – A European Journal, EarlyView.
Photochemical activation of N‐phenylphenothiazine (PPT) enables a selective direct benzene amination with hydroxylamine in the presence of various vanadium catalysts under mild reaction conditions. Spectroscopic and kinetic analyses identify a key vanadium(IV)‐hydroxylamine intermediate, elucidate the crucial roles of the acidic medium, the ...
Dana Králová   +6 more
wiley   +1 more source

Revisiting C4N4 Fluorophore: Theoretical Elucidation of the Origin of Fluorescent Properties of 2,5‐Diaminopyrimidines and Strategic Applications to Pd Detection

open access: yesChemistry – A European Journal, EarlyView.
A compact C4N4 fluorophore—comprising only four carbons and four nitrogens—shows structure‐dependent fluorescence that can be rationalized by TDDFT and AFIR analyses. Rational structural design controls whether emission is turned ON or OFF through computationally identified CI structures.
Miki Kohei   +5 more
wiley   +1 more source

Electrochemical Disposal of Hydrazines in Water [PDF]

open access: yes
An electrochemical method of disposal of hydrazines dissolved in water has been devised. The method is applicable to hydrazine (N2H4), to monomethyl hydrazine [also denoted by MMH or by its chemical formula, (CH3)HNNH2], and to unsymmetrical dimethyl ...
Andrews, Craig   +6 more
core   +1 more source

Electrochemical behaviour of dimethyl hydrazones - part – 1 cyclohexanone dimethyl hydrazone [PDF]

open access: yes, 1986
The polarographic behaviour of cyclohexanone dimethyl hydrazone at dropping mercury electrode in aqueous alcoholic medium has been investigated in presence of 0.1 M KC1 as supportingelectrolyle.The effect of depolariser concentration, pH, and drop time
Rawat, N.S.   +2 more
core  

Synthetic Strategies for Activity‐Based Probes to Decode Ubiquitin‐Like Modifiers

open access: yesChemistry – A European Journal, EarlyView.
ABSTRACT Ubiquitin‐like proteins (Ubls) such as SUMO, NEDD8, ISG15, URM1, UFM1, FAT10, ATG8/ATG12, and FUBI are essential regulators of cellular homeostasis, controlling processes from protein stability and trafficking to immune signaling and autophagy.
Saibal Chanda   +5 more
wiley   +1 more source

Iodophor-Catalyzed Disulfenylation of Amino Naphthalenes with Aryl Sulfonyl Hydrazines

open access: yesMolecules
An iodophor-catalyzed direct disulfenylation of amino naphthalenes with aryl sulfonyl hydrazines in water was developed. A series of aryl sulfides were obtained in moderate to excellent yields.
Yutong Yuan   +4 more
doaj   +1 more source

Asymmetric Reduction of Unactivated Alkenes

open access: yesChemistry – A European Journal, EarlyView.
Unactivated alkenes rank among the most inert functional groups in synthesis and their selective reduction remains challenging. This Review charts the evolution from classical metal‐catalyzed hydrogenation to radical hydrogen atom transfer (HAT) and emerging biocatalytic concepts, highlighting how complementary mechanistic strategies, including the ...
Nico D. Fessner   +3 more
wiley   +1 more source

HYDRAZINE [PDF]

open access: yesThe Annals of Occupational Hygiene, 1978
openaire   +3 more sources

Monosubstituted N‐Arylhydroxylamine Chemistry: Integrating Contemporary Synthetic Approaches for the Efficient Construction of Diverse Heterocyclic Scaffolds

open access: yesChemistry – A European Journal, EarlyView.
Monosubstituted N‐arylhydroxylamines represent a unique subclass of hydroxylamines that act as pivotal intermediates in redox transformations and as versatile platforms for further synthetic transformations. They serve as key building blocks in the synthesis of architecturally complex heterocycles and other valuable organic compounds.
Michael G. Kallitsakis   +2 more
wiley   +1 more source

Heterocyclic synthesis with ω-bromoacetophenone: Synthesis of some new pyrazole, pyridazine and furan derivatives [PDF]

open access: yes, 2008
p-Bromophenacylnitrile derivatives 3a,b react with hydrazinederivatives under different conditions to afford the diaminopyrazoles 4a,b, the pyridazine-6-imines 5a,b,and 5-aminopyrazoles 11a,b.
Abdallah, Tayseer A.   +2 more
core  

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