Results 1 to 10 of about 60,285 (147)

Highly Selective Electrocatalytic Oxidation of Amines to Nitriles Assisted by Water Oxidation on Metal-Doped α-Ni(OH)2.

open access: yesJournal of the American Chemical Society, 2022
Selective oxidation to synthesize nitriles is critical for feedstock manufacturing in the chemical industry. Current strategies typically involve substitutions of alkyl halides with toxic cyanides or the use of strong oxidation reagents (oxygen or ...
Yuxia Sun   +10 more
semanticscholar   +1 more source

Nickel-catalyzed hydrogenative coupling of nitriles and amines for general amine synthesis

open access: yesScience, 2022
Efficient and general methods for the synthesis of amines remain in high demand in the chemical industry. Among the many known processes, catalytic hydrogenation is a cost-effective and industrially proven reaction and currently used to produce a wide ...
V. Chandrashekhar   +3 more
semanticscholar   +1 more source

Efficient iron single-atom catalysts for selective ammoxidation of alcohols to nitriles

open access: yesNature Communications, 2022
Zeolitic imidazolate frameworks derived Fe1-N-C catalysts with isolated single iron atoms have been synthesized and applied for selective ammoxidation reactions.
Kangkang Sun   +4 more
semanticscholar   +1 more source

An enzyme-mimic single Fe-N3 atom catalyst for the oxidative synthesis of nitriles via C─C bond cleavage strategy

open access: yesScience Advances, 2022
The cleavage and functionalization of recalcitrant carbon─carbon bonds is highly challenging but represents a very powerful tool for value-added transformation of feedstock chemicals.
Jingzhong Qin   +9 more
semanticscholar   +1 more source

Silica-supported Fe/Fe–O nanoparticles for the catalytic hydrogenation of nitriles to amines in the presence of aluminium additives

open access: yesNature Catalysis, 2021
The hydrogenation of nitriles to amines represents an important and frequently used industrial process due to the broad applicability of the resulting products in chemistry and life sciences.
V. Chandrashekhar   +8 more
semanticscholar   +1 more source

The ALMA-PILS survey: complex nitriles towards IRAS 16293–2422 [PDF]

open access: yesAstronomy & Astrophysics, 2018
Context. Complex organic molecules are readily detected in the inner regions of the gaseous envelopes of forming protostars. Their detection is crucial to understanding the chemical evolution of the Universe and exploring the link between the early ...
H. Calcutt   +10 more
semanticscholar   +1 more source

Quasi Pd1Ni single-atom surface alloy catalyst enables hydrogenation of nitriles to secondary amines

open access: yesNature Communications, 2019
Hydrogenation of nitriles represents as an atom-economic route to synthesize amines, crucial building blocks in fine chemicals. However, high redox potentials of nitriles render this approach to produce a mixture of amines, imines and low-value ...
Hengwei Wang   +11 more
semanticscholar   +1 more source

Nitromethane as a nitrogen donor in Schmidt-type formation of amides and nitriles

open access: yesScience, 2019
Sourcing nitrogen from nitromethane Nitromethane is produced in bulk quantities for use as a solvent. Its applications as a reagent have focused mainly on the acidity of the methyl protons en route to modifying the carbon center. Liu et al. now report an
Jianzhong Liu   +8 more
semanticscholar   +1 more source

Delayed catalyst function enables direct enantioselective conversion of nitriles to NH2-amines

open access: yesScience, 2019
Amines emerge, as copper bides its time Concurrent operation of two or more catalytic cycles requires a delicate balance of relative rates. Zhang et al. developed an amine synthesis in which allenes and nitriles are coupled under reductive conditions.
Shaochen Zhang   +5 more
semanticscholar   +1 more source

Sustainable Alkylation of Nitriles with Alcohols by Manganese Catalysis.

open access: yesJournal of Organic Chemistry, 2019
A general and chemoselective catalytic alkylation of nitriles using a homogeneous nonprecious manganese catalyst is presented. This alkylation reaction uses naturally abundant alcohols and readily available nitriles as coupling partners.
Jannik C Borghs   +4 more
semanticscholar   +1 more source

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