Results 31 to 40 of about 3,282 (218)
Neue Methode zur reduktiven Desaminierung primärer aliphatischer Amine
A new method for reductive deamination of primary aliphatic amines via tributyltin hydride reduction of aromatic imidoyl chlorides is reported. Good yields of hydrocarbons were obtained from benzylamines and cyclohexylamine, but not from 1-alkylamines.
Thomas Wirth, Christoph Rüchardt
doaj +1 more source
A series of novel urea, sulfamide and N,N-dipropargyl substituted benzylamines were synthesized from dihydrochalcones. The synthesized compounds were evaluated for their cholinesterases and carbonic anhydrase inhibitory actions.
Göksu, Süleyman +5 more
core +1 more source
Leigh's metal‐free active template‐based SNAr of an amine on halogenopyridiniums, in the presence of a crown ether, successfully afforded 4‐aminopyridinium‐containing rotaxanes. Further molecular machinery was carried out by deprotonation‐then‐carbamoylation of the conjugated amino moiety.
Ivaylo Stoyanov +2 more
wiley +2 more sources
Carbon Dioxide-Mediated C(sp2)–H Arylation of Primary and Secondary Benzylamines
Carbon-carbon bond formation by transition metal-catalyzed C–H activation has become an important strategy to fabricate new bonds in a rapid fashion.
Mohit, Kapoor +2 more
core +2 more sources
17β-Hydroxysteroid dehydrogenase type 3 (17β-HSD3) is expressed at high levels in testes and seminal vesicles; it is also present in prostate tissue and involved in gonadal and non-gonadal testosterone biosynthesis.
Nigel Vicker +7 more
doaj +1 more source
Conventional quinazoline synthesis methods involve a highly multistep reaction, and often require excess amounts of substrate to control the product selectivity, leading to significant resource wastage.
Yuki Yamamoto +7 more
doaj +1 more source
Direct Palladium-Catalyzed Ortho-Arylation of Benzylamines
Unsubstituted benzylamines and N-methylbenzylamine can be ortho-arylated under palladium catalysis at 130 °C.
Anna Lazareva (2236426) +1 more
core +2 more sources
Influence of the organic linker substituent on the catalytic activity of MIL-101(Cr) for the oxidative coupling of benzylamines to imines [PDF]
MIL-101(Cr) having substituents at the terephthalate linker (X = H, NO2, SO3H, Cl, CH3 and NH2) promotes the aerobic oxidation of benzylamines to the corresponding N-benzylidene benzylamines at different rates.
García Gómez, Hermenegildo +4 more
core +2 more sources
A new effective method for the construction of nitrogen heterocycles incorporating endocyclic pharmacophore sulfonamide fragment, based on the use of easy accessible N-(chlorosulfonyl)imidoyl chloride, CCl3C(Cl)=NSO2Cl (1), has been developed.
Oleksandr Shalimov +3 more
doaj +1 more source
Photocatalysis is accepted as a promising method for selective oxidative coupling of amine to imine. However, owing to the rapid dehydrogenation of the generated imine intermediate of α‐amino hydrogen to butyronitrile, it remains a huge challenge to ...
Chuntao Wang +5 more
doaj +1 more source

