53263-53-9

Upstream product

• 7148-07-4 1-pyrrolidinocyclopent-1-ene 
• 2207-96-7 methyl 2-phenyldiazene-1-carboxylate 
• 1614-92-2 1-(N-piperidino)cyclopentene 
• 936-52-7 1-(N-morpholino)cyclopent-1-ene 
• 4177-25-7 1-cyclopent-1-enyl-4-phenyl-piperazine 
• 106690-05-5 Benzoic acid N'-phenyl-N'-(2-pyrrolidin-1-yl-cyclopent-1-enyl)-hydrazide 
• 106690-03-3 Benzoic acid N'-phenyl-N'-(2-piperidin-1-yl-cyclopent-2-enyl)-hydrazide 
• 106689-99-0 Benzoic acid N'-(2-morpholin-4-yl-cyclopent-1-enyl)-N'-phenyl-hydrazide 
• 100-65-2 N-Phenylhydroxylamine 
• 120-92-3 cyclopentanone 
• 952-53-4 (E)-phenyl(phenyldiazenyl)methanone 
• 62-53-3 aniline 
• 69381-32-4 2-iodocyclopentanone 

Relevant academic research and scientific papers

Copper-catalyzed amination of alkenes and ketones by phenylhydroxylamine

The catalytic activity of a number of copper complexes and salts toward allylic amination of alkenes using phenylhydroxylamine as the nitrogen fragment donor has been investigated. The best catalyst is CuCl2·2H2O, which produces moderate yields of allylamines with high regioselectivity resulting from double bond transposition. A mechanism similar to that for the molybdenum and the FePc systems is proposed. The first step in the catalytic cycle is the formation of nitrosobenzene from the oxidation of phenylhydroxylamine by Cu(II). The next step is an ene reaction of the alkene with PhNO to produce an allylhydroxylamine, which is then reduced to the allylamine product by Cu(I), thus regenerating Cu(II). The same system can also transfer the nitrogen fragment to the α-carbon of cyclic ketones; this is accompanied by dehydrogenation in some cases to produce α-aminated, α,β-unsaturated ketones.

Multifunctionalization of Unactivated Cyclic Ketones via an Electrochemical Process: Access to Cyclic α-Enaminones

The multifunctionalization of unactivated cyclic ketones was developed via an electrochemically intermolecular α-amination under metal-free conditions. The reaction can be carried out smoothly with a broad scope of the aromatic amines substrates under mil

REACTIVITY OF CYCLOPENTANONE ENAMINES TOWARDS NON-SYMMETRIC ELECTROPHILIC DIAZENES

The non-symmetric electrophilic diazenes 2 and 3 react with 1-aminocyclopentenes 1 giving enamine adducts exclusively, which have been isolated in some cases; on hydrolysis, the hydrazine substituents in the monoadducts from 2 is cleaved and only α,β-unsa

REACTIVITY OF CYCLOPENTANONE ENAMINES TOWARDS ACYL ARYLDIAZENES

Reactions of 1-aminocyclopentenes 1 with acyl aryldiazenes 2 give 1:1 enaminic adducts 3 and 4, or 1,3,4-oxadiazines 5.Isolation of these products was not always possible in the reactions of 1-(piperidin-1-yl)- and 1-(pyrrolidin-1-yl)-cyclopentene.Acidic hydrolysis gave 2-(N-acyl-N'-aryl)hydrazinocyclopentanones 6 or 2-arylaminocyclopentenones 8, depending upon the amino moiety and the cyclic or open chain nature of the adducts.