Results 61 to 70 of about 22,537 (233)

Switching polymorph stabilities with impurities provides a thermodynamic route to benzamide form III

open access: yesCommunications Chemistry, 2021
The formation of solid solutions can result in changes of relative stabilities of crystal polymorphs. Here, the elusive form III of benzamide is stabilized through solid solution formation with nicotinamide.
Weronika Kras   +4 more
doaj   +1 more source

The 68Ga-labeled chlorinated benzamide derivative: A novel PET imaging probe for detection of melanoma

open access: yesResults in Chemistry
The benzamide structure is known for its ability to target melanin, a specific biomarker of melanoma. Therefore, we developed a new chlorinated benzamide structure for the detection of melanoma on positron emission tomography (PET). The derived benzamide
Yejin Seo   +9 more
doaj   +1 more source

2-Amino-N-(2-chloropyridin-3yl)benzamide

open access: yesIUCrData, 2017
The title compound, C12H10ClN3O, is a condensation product of 3-amino-2-chloropyridine and ethyl 2-aminobenzoate in which the aromatic rings are almost coplanar [dihedral angle = 2.28 (9)°] and an intramolecular N—H...O hydrogen bond occurs.
Noura M. Riad   +2 more
doaj   +1 more source

Dual‐Function Electrocatalysis: Simultaneous Wastewater Remediation and Hydrogen Evolution—A Comprehensive Review

open access: yesCarbon Energy, EarlyView.
Replacing the oxygen evolution reaction with the electro‐oxidation of pollutants and waste streams offers an energy‐efficient route for simultaneous hydrogen production and pollutant remediation. This review summarizes the reaction mechanisms, catalyst design principles, and emerging paired‐electrolysis strategies that govern activity, selectivity ...
Safa Al‐Yahyaey   +4 more
wiley   +1 more source

The Mechanism of Visible‐Light Photochemical Rearrangements of Conjugated Amide Enolates

open access: yesChemistry – A European Journal, EarlyView.
Visible light irradiation of extended enolates of N‐benzylamides leads to homolytic C─N Bond cleavage, generating a biradical. Computational and mechanistic studies suggest rapid radical recombination within a solvent cage to give either ring‐expanded or rearranged products. ABSTRACT Deprotonation of conjugated amides forms colored solutions of lithium
James Mortimer   +3 more
wiley   +1 more source

Benzamide coordination compounds of magnesium nicotinate [PDF]

open access: yes, 2019
The synthesis of benzamide coordination compounds of magnesium nicotinate by a mechanochemical method was carried out. The optimal component ratios and the time of the reactions were established.
Мavluda, Ibragimova   +1 more
core  

Synthesis of benzamide derivatives and their evaluation as antiprion agents

open access: yes, 2012
A new set of 5-(2-(pyrrolidin-1-yl)acetamido)-N-butyl-2-(substituted)benzamide and 5-(2-(piperidin-1-yl)acetamido)-N-butyl-2-(substituted) benzamide derivatives were synthesized in which as structural features the 2-(1-pyrrolidinyl)- or 2-(1-piperidyl ...
H. A. Kretzschmar   +14 more
core   +1 more source

Cobalt‐Catalyzed C(sp3)H Carbonylation Enabled by Mo(CO)6

open access: yesEuropean Journal of Organic Chemistry, EarlyView.
Cobalt‐catalyzed carbonylative C(sp3)H cyclization of aliphatic amides using Mo(CO)6 as a solid CO surrogate enables efficient access to substituted succinimides under operationally simple conditions. The carbonylation of unactivated C(sp3)H bonds represents an attractive strategy for the synthesis of valuable carbonyl‐containing compounds.
Emma Duro   +4 more
wiley   +1 more source

Synthesis of telechelic poly(p-benzamide)s [PDF]

open access: yes, 2018
Well-defined telechelic poly(benzamide)s were synthesized by chain-growth polycondensation of phenyl-4-amino benzoate and pentafluorophenyl-4-amino benzoate derivatives with a bifunctional initiator in the presence of LiTMP as base. The polymerization
Mahshid Alizadeh   +4 more
core   +1 more source

Expanding the Scope of 1,2‐Diazepines Through Alternative Activation Strategies

open access: yesEuropean Journal of Organic Chemistry, EarlyView.
Often overlooked due to tedious synthetic routes, 1,2‐diazepines can be found in handful of biorelevant molecules. Previous reports from our group lifted the principal synthetic lock: a rapid and user‐friendly protocol to reach monocyclic 1,2‐diazepines from readily available pyridines and electrophilic activating groups. Herein, we extend the scope of
Alexis Leblais   +4 more
wiley   +1 more source

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