Results 71 to 80 of about 28,244 (201)
Nitrogen Abstraction from Nitriles by Osmium(IV) Complexes
, 2016 Nitrogen Abstraction from Nitriles by Osmium(IV ...
Scott Lovell (122251) +2 more
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Preparation of 5-Substituted 1H-Tetrazoles from Nitriles in Water†
, 2016 The addition of sodium azide to nitriles to give 1H-tetrazoles is shown to proceed readily in water with zinc salts as catalysts. The scope of the reaction is quite broad; a variety of aromatic nitriles, activated and unactivated alkyl nitriles ...
Zachary P. Demko (330506) +1 more
core +1 more source
SYNTHESIS OF DERIVATIVES OF MERCAPTO AMIDINES AMIDES AND NITRILES.
, 1963 SYNTHESIS OF DERIVATIVES OF MERCAPTO AMIDINES AMIDES AND ...
THOMAS LAURENCE. WELSH (7977872)
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Ruthenium-Catalyzed Hydrogenation of Nitriles: Insights into the Mechanism
, 2016 Ruthenium-Catalyzed Hydrogenation of Nitriles: Insights into the ...
Rebeca Reguillo (2291329) +4 more
core +3 more sources
Molecules, 2015 The Schmidt reaction of aromatic aldehydes using a substoichiometric amount (40 mol %) of triflic acid is described. Low catalyst loading was enabled by a strong hydrogen-bond-donating solvent hexafluoro-2-propanol (HFIP).
Hashim F. Motiwala +2 more
doaj +1 more source
Table_4_Impact of Nitriles on Bacterial Communities.XLSX
, 2019 Nitriles are organic molecules with –C≡N as functional group and often toxic for living organisms. Detoxification can occur via nitrilases that degrade nitriles directly to carboxylic acids and ammonia, or with nitrile hydratases and amidases that ...
Robert Hertel (712769) +4 more
core +1 more source
Metal-Mediated Addition of N-Nucleophiles to Isocyanides: Mechanistic Aspects
Molecules, 2017 Despite the long history of the investigation of nucleophilic addition to metal-bound isocyanides, some important aspects of the reaction mechanism remain unclear even for the simplest systems.
Maxim L. Kuznetsov, Vadim Yu. Kukushkin
doaj +1 more source
ω-Halonitriles: Domino Cyclizations to Oxa- and Carbocyclic Nitriles
, 2016 t-BuOK-induced deprotonation of ω-haloalkylnitriles generates remarkably stable potassiated nitriles. In situ deprotonation and alkylation of ω-chloroalkylnitriles with aldehyde electrophiles trigger sequential nucleophilic−electrophilic alkylations ...
Venugopal Gudipati (2533285) +2 more
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, 2016 Reaction of α-Amidoalkylphenyl Sulfones with Lithiated Nitriles: Syn-Selective Synthesis of β-Amino ...
Roberto Profeta (2276374) +2 more
core +3 more sources
Molecules, 2009 Aromatic aldehydes bearing electron-donating groups are easily converted into their respective nitriles using NH2OH·HCl and TiO2 under microwave irradiation, while those bearing an electron-withdrawing group give the corresponding oximes.
Lucas Villas-Boas Hoelz +3 more
doaj +1 more source