88785-71-1Relevant articles and documents
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