TY - BOOK ID - 145964796 TI - Nitrogen-Containing Molecules: Natural and Synthetic Products Including Coordination Compounds AU - Matiadis, Dimitrios AU - Halevas, Eleftherios PY - 2021 PB - Basel, Switzerland MDPI - Multidisciplinary Digital Publishing Institute DB - UniCat KW - Research & information: general KW - heterocycle KW - piperazine KW - pyrimidine KW - DABCO KW - nucleophilic displacement KW - chlorination KW - [1,3]-H shift KW - aza-Michael addition KW - DFT calculations KW - dimethyl acetylenedicarboxylate KW - isoxazolo[3,4-b]quinolin-3(1H)-one KW - pyrazolines KW - curcuminoids KW - nitrogen heterocycles KW - cytotoxic KW - DNA binding KW - MDR reversal KW - oxygen-nitrogen heterocycles KW - 11a,12-dihydrobenzo[b]benzo[5,6][1,4]oxazino[2,3-e][1,4]oxazine KW - disulfur dichloride KW - o-aminophenol KW - condensation KW - 4-anilino-quin(az)olines KW - hinge binder KW - conformational flexibility KW - kinase inhibitor design KW - imine KW - Schiff base KW - X-ray crystallographic analysis KW - Cu(II) complex KW - gamma-amino acid KW - ruthenium KW - carbonyl complex KW - azopyridine KW - anion radical KW - electronic structure KW - magnetic properties KW - chalcogenophene KW - heterocycles KW - ligands KW - pyridine derivatives KW - thiophene derivatives KW - aminocyclopentitol KW - bicyclic aziridine KW - water chemistry KW - nucleophilic substitution KW - homopiperazine KW - X-ray structure KW - C-C bond length KW - 15N-NMR KW - catechol KW - alkyne KW - thiol-alkyne click reaction KW - domino reactions KW - bromination KW - intramolecular SN displacement KW - carbocyclic hydantoins KW - N-1 substituted hydantoin KW - spiro hydantoins KW - imidazolidine-2,4-diones KW - stereochemistry KW - NMR KW - HRMS KW - GIAO KW - ring closing KW - Au-nanoparticles KW - NaBH4 KW - amino-substituted fused oxazolocoumarin KW - fused oxazolocoumarins KW - chemoselective reduction KW - o-hydroxynitrocoumarins KW - benzimidazole KW - nucleophilic aromatic substitution KW - thiosemicarbazone KW - heterocycle KW - piperazine KW - pyrimidine KW - DABCO KW - nucleophilic displacement KW - chlorination KW - [1,3]-H shift KW - aza-Michael addition KW - DFT calculations KW - dimethyl acetylenedicarboxylate KW - isoxazolo[3,4-b]quinolin-3(1H)-one KW - pyrazolines KW - curcuminoids KW - nitrogen heterocycles KW - cytotoxic KW - DNA binding KW - MDR reversal KW - oxygen-nitrogen heterocycles KW - 11a,12-dihydrobenzo[b]benzo[5,6][1,4]oxazino[2,3-e][1,4]oxazine KW - disulfur dichloride KW - o-aminophenol KW - condensation KW - 4-anilino-quin(az)olines KW - hinge binder KW - conformational flexibility KW - kinase inhibitor design KW - imine KW - Schiff base KW - X-ray crystallographic analysis KW - Cu(II) complex KW - gamma-amino acid KW - ruthenium KW - carbonyl complex KW - azopyridine KW - anion radical KW - electronic structure KW - magnetic properties KW - chalcogenophene KW - heterocycles KW - ligands KW - pyridine derivatives KW - thiophene derivatives KW - aminocyclopentitol KW - bicyclic aziridine KW - water chemistry KW - nucleophilic substitution KW - homopiperazine KW - X-ray structure KW - C-C bond length KW - 15N-NMR KW - catechol KW - alkyne KW - thiol-alkyne click reaction KW - domino reactions KW - bromination KW - intramolecular SN displacement KW - carbocyclic hydantoins KW - N-1 substituted hydantoin KW - spiro hydantoins KW - imidazolidine-2,4-diones KW - stereochemistry KW - NMR KW - HRMS KW - GIAO KW - ring closing KW - Au-nanoparticles KW - NaBH4 KW - amino-substituted fused oxazolocoumarin KW - fused oxazolocoumarins KW - chemoselective reduction KW - o-hydroxynitrocoumarins KW - benzimidazole KW - nucleophilic aromatic substitution KW - thiosemicarbazone UR - https://www.unicat.be/uniCat?func=search&query=sysid:145964796 AB - A total of 16 original research articles. Contributions from 10 countries from 3 continents. Organic synthesis towards novel heterocyclic compounds. Fully characterized inorganic and organic molecules including X-ray crystallographic analysis. Cyclization reactions, reactivity of aromatic compounds and improved synthetic methodologies of important intermediate compounds. ER -