40468-86-8Relevant articles and documents
193. Photoformation of (Z)-Isomers in Diarylazomethines. Part IV. Direct and Sensitized Photoisomerization of Pyridyl Analogues of Benzylidene-aniline and Absorption Spectra of their (Z)-Isomers
Maeda, Koko,Fischer, Ernst
, p. 1961 - 1965 (1983)
UV irradiation of solutions of the (E)-isomers of five (out of the possible six) monopyridyl analogues at reduced temperatures results in extensive (80-90percent) conversion into the corresponding (Z)-isomers.The process is reversible both thermally and photochemically.The (Z)-isomers are stable at temperatures below -80 deg, and their absorption spectra were estimated.Biacetyl-photosensitized (E)->(Z) isomerization was observed, with (Z)-contents of ca. 70percent at the photostationary state.
Superelectrophilic Diels–Alder reactions and oxidations leading to heterocyclic biaryl compounds
Vuong, Hien,Klumpp, Douglas A.
supporting information, p. 316 - 323 (2019/01/18)
Heterocyclic imines provide biaryl products by a two-step transformation. The first transformation involves a Diels–Alder reaction with a multiply protonated imine to give a tetrahydroquinoline product, whereas the second step involves oxidation with elem
Diels-Alder Reactions with Ethylene and Superelectrophiles
Vuong, Hien,Dash, Barada P.,Nilsson Lill, Sten O.,Klumpp, Douglas A.
supporting information, p. 1849 - 1852 (2018/04/16)
Diels-Alder reactions have been accomplished with ethylene as the dienophile through the use of inverse-electron demand Diels-Alder chemistry. As a key aspect of the chemistry, the dienes are part of tri- or dicationic superelectrophilic systems. Theoreti
Silver(I)-pyridinyl Schiff base complexes: Synthesis, characterisation and antimicrobial studies
Njogu, Eric M.,Omondi, Bernard,Nyamori, Vincent O.
, p. 118 - 128 (2017/02/05)
Fifteen new silver(I)-pyridinyl complexes of the general formula [AgL2]X, where X = ClO4?, OTf or NO3?, were synthesised by reacting (E)-N-(pyridinylmethylene)aniline ligands and the respective silver