Nitrogen-Containing Molecules: Natural and Synthetic Products Including Coordination Compounds

• Format: eBook
• Language: English
• Published: Basel, Switzerland MDPI - Multidisciplinary Digital Publishing Institute 2021
• Subjects: Research & information: general; [1,3]-H shift; 11a,12-dihydrobenzo[b]benzo[5,6][1,4]oxazino[2,3-e][1,4]oxazine; 15N-NMR; 4-anilino-quin(az)olines; alkyne; amino-substituted fused oxazolocoumarin; aminocyclopentitol; anion radical; Au-nanoparticles; aza-Michael addition; azopyridine; benzimidazole; bicyclic aziridine; bromination; C-C bond length; carbocyclic hydantoins; carbonyl complex; catechol; chalcogenophene; chemoselective reduction; chlorination; condensation; conformational flexibility; Cu(II) complex; curcuminoids; cytotoxic; DABCO; DFT calculations; dimethyl acetylenedicarboxylate; disulfur dichloride; DNA binding; domino reactions; electronic structure; fused oxazolocoumarins; gamma-amino acid; GIAO; heterocycle; heterocycles; hinge binder; homopiperazine; HRMS; imidazolidine-2,4-diones; imine; intramolecular SN displacement; isoxazolo[3,4-b]quinolin-3(1H)-one; kinase inhibitor design; ligands; magnetic properties; MDR reversal; N-1 substituted hydantoin; n/a; NaBH4; nitrogen heterocycles; NMR; nucleophilic aromatic substitution; nucleophilic displacement; nucleophilic substitution; o-aminophenol; o-hydroxynitrocoumarins; oxygen-nitrogen heterocycles; piperazine; pyrazolines; pyridine derivatives; pyrimidine; ring closing; ruthenium; Schiff base; spiro hydantoins; stereochemistry; thiol-alkyne click reaction; thiophene derivatives; thiosemicarbazone; water chemistry; X-ray crystallographic analysis; X-ray structure
• Online Access: Open Access: DOAB: description of the publication; Open Access: DOAB, download the publication
• Physical Description: 1 online resource (124 p.)
• ISBN: 9783036522579; 9783036522586; books978-3-0365-2258-6
• Access: Open Access

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.