Results 51 to 60 of about 26,755 (292)
Branch-Selective Addition of Unactivated Olefins into Imines and Aldehydes [PDF]
, 2018 Radical hydrofunctionalization occurs with ease using met-al-hydride atom transfer (MHAT) catalysis to couple alkenes and competent radicalophilic electrophiles. Traditional two-electron electrophiles have remained unreactive.
Suhelen, Vásquez-Céspedes +4 more
core +1 more source
Synthesis and enantioselective hydrogenation of seven-membered cyclic imines: substituted dibenzo[b,f][1,4]oxazepines [PDF]
, 2011 Synthesis and enantioselective hydrogenation of seven-membered cyclic imines: substituted dibenzo[b,f][1,4]oxazepinesHighly enantioselective hydrogenation of seven-membered cyclic imines, substituted dibenzo[b,f][1,4]oxazepines, was achieved, with up to ...
Li, Wei +6 more
core +1 more source
Molecules, 2021 A series of (E)-4-bromo-N-((3-bromothiophen-2-yl)methylene)-2-methylaniline analogs synthesized in considerable yields through Suzuki cross-coupling reactions.
Komal Rizwan +6 more
doaj +1 more source
Reduction of Secondary Amides to Imines Catalysed by Schwartz’s Reagent [PDF]
, 2022 The partial reduction of amides is a challenging transformation that must overcome the intrinsic stability of the amide bond, a ubiquitous motif in organic chemistry, and exhibit high chemoselective control.
Liam, Donnelly +2 more
core +1 more source
Molecules, 2020 Inversions in the periselectivity of formal aza-Diels–Alder cycloadditions between α-oxoketenes generated by a thermally-induced Wolff rearrangement and 1-azadienes were observed experimentally as a function of the α-oxoketene and the 1-azadiene, as well
Marc Presset +4 more
doaj +1 more source
Rhodium-Catalyzed Addition of Boronic Acids to Vinylogous Imines Generated in situ from Sulfonylindoles [PDF]
, 2011 Rhodium-Catalyzed Addition of Boronic Acids to Vinylogous Imines Generated in situ from SulfonylindolesThe rhodium-catalyzed addition of arylboronic acids to vinylogous imines generated in situ from sulfonylindoles has been developed.
江国防 +5 more
core +1 more source
Determination of Stability for imines derived from carbonyl compounds by conductivity measurements
Tikrit Journal of Pure Science, 2018 The project explained for the first time, how conductivity method was used in the determination of stability of some imines derived from mother compounds 2-acetyl pyridine, 3 or 4 –hydroxy benzaldehyde, and others. The method as found, simple precise
A.S.P. Azzouz, D.B.AL-Bakzo
doaj +1 more source
Current Opinion in Chemical Biology, 2017 Imine reductases (IREDs) have emerged as a valuable new set of biocatalysts for the asymmetric synthesis of optically active amines. The development of bioinformatics tools and searchable databases has led to the identification of a diverse range of new IRED biocatalysts that have been characterised and employed in different synthetic processes.
Mangas-Sanchez, Juan +8 more
openaire +4 more sources
Schiff Bases: Interesting Scaffolds with Promising Antitumoral Properties
Applied Sciences, 2021 Schiff bases, named after Hugo Schiff, are highly reactive organic compounds broadly used as pigments and dyes, catalysts, intermediates in organic synthesis, and polymer stabilizers.
Domenico Iacopetta +6 more
doaj +1 more source
Molecules, 1998 The synthesis of eight hydroxy- and 2-oxopyranochromone-3-carboxaldehydes 3, 5 and their reactions with 2-hydroxyaniline, 2,4-dinitrophenylhydrazine and 2-benzothiazolylhydrazine were investigated.
Hafez M. El-Shaaer +4 more
doaj +1 more source