Nitrogen-Containing Molecules: Natural and Synthetic Products Including Coordination Compounds
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...
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| Format: | Book Chapter |
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Basel, Switzerland
MDPI - Multidisciplinary Digital Publishing Institute
2021
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| Online Access: | Get Fullteks DOAB: description of the publication |
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| LEADER | 04147naaaa2201201uu 4500 | ||
|---|---|---|---|
| 001 | doab_20_500_12854_76919 | ||
| 005 | 20220111 | ||
| 020 | |a books978-3-0365-2258-6 | ||
| 020 | |a 9783036522579 | ||
| 020 | |a 9783036522586 | ||
| 024 | 7 | |a 10.3390/books978-3-0365-2258-6 |c doi | |
| 041 | 0 | |a English | |
| 042 | |a dc | ||
| 072 | 7 | |a GP |2 bicssc | |
| 100 | 1 | |a Matiadis, Dimitrios |4 edt | |
| 700 | 1 | |a Halevas, Eleftherios |4 edt | |
| 700 | 1 | |a Matiadis, Dimitrios |4 oth | |
| 700 | 1 | |a Halevas, Eleftherios |4 oth | |
| 245 | 1 | 0 | |a Nitrogen-Containing Molecules: Natural and Synthetic Products Including Coordination Compounds |
| 260 | |a Basel, Switzerland |b MDPI - Multidisciplinary Digital Publishing Institute |c 2021 | ||
| 300 | |a 1 electronic resource (124 p.) | ||
| 506 | 0 | |a Open Access |2 star |f Unrestricted online access | |
| 520 | |a 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. | ||
| 540 | |a Creative Commons |f https://creativecommons.org/licenses/by/4.0/ |2 cc |4 https://creativecommons.org/licenses/by/4.0/ | ||
| 546 | |a English | ||
| 650 | 7 | |a Research & information: general |2 bicssc | |
| 653 | |a heterocycle | ||
| 653 | |a piperazine | ||
| 653 | |a pyrimidine | ||
| 653 | |a DABCO | ||
| 653 | |a nucleophilic displacement | ||
| 653 | |a chlorination | ||
| 653 | |a [1,3]-H shift | ||
| 653 | |a aza-Michael addition | ||
| 653 | |a DFT calculations | ||
| 653 | |a dimethyl acetylenedicarboxylate | ||
| 653 | |a isoxazolo[3,4-b]quinolin-3(1H)-one | ||
| 653 | |a pyrazolines | ||
| 653 | |a curcuminoids | ||
| 653 | |a nitrogen heterocycles | ||
| 653 | |a cytotoxic | ||
| 653 | |a DNA binding | ||
| 653 | |a MDR reversal | ||
| 653 | |a oxygen-nitrogen heterocycles | ||
| 653 | |a 11a,12-dihydrobenzo[b]benzo[5,6][1,4]oxazino[2,3-e][1,4]oxazine | ||
| 653 | |a disulfur dichloride | ||
| 653 | |a o-aminophenol | ||
| 653 | |a condensation | ||
| 653 | |a 4-anilino-quin(az)olines | ||
| 653 | |a hinge binder | ||
| 653 | |a conformational flexibility | ||
| 653 | |a kinase inhibitor design | ||
| 653 | |a imine | ||
| 653 | |a Schiff base | ||
| 653 | |a X-ray crystallographic analysis | ||
| 653 | |a Cu(II) complex | ||
| 653 | |a gamma-amino acid | ||
| 653 | |a ruthenium | ||
| 653 | |a carbonyl complex | ||
| 653 | |a azopyridine | ||
| 653 | |a anion radical | ||
| 653 | |a electronic structure | ||
| 653 | |a magnetic properties | ||
| 653 | |a chalcogenophene | ||
| 653 | |a heterocycles | ||
| 653 | |a ligands | ||
| 653 | |a pyridine derivatives | ||
| 653 | |a thiophene derivatives | ||
| 653 | |a aminocyclopentitol | ||
| 653 | |a bicyclic aziridine | ||
| 653 | |a water chemistry | ||
| 653 | |a nucleophilic substitution | ||
| 653 | |a homopiperazine | ||
| 653 | |a X-ray structure | ||
| 653 | |a C-C bond length | ||
| 653 | |a 15N-NMR | ||
| 653 | |a catechol | ||
| 653 | |a alkyne | ||
| 653 | |a thiol-alkyne click reaction | ||
| 653 | |a domino reactions | ||
| 653 | |a bromination | ||
| 653 | |a intramolecular SN displacement | ||
| 653 | |a carbocyclic hydantoins | ||
| 653 | |a N-1 substituted hydantoin | ||
| 653 | |a spiro hydantoins | ||
| 653 | |a imidazolidine-2,4-diones | ||
| 653 | |a stereochemistry | ||
| 653 | |a NMR | ||
| 653 | |a HRMS | ||
| 653 | |a GIAO | ||
| 653 | |a ring closing | ||
| 653 | |a Au-nanoparticles | ||
| 653 | |a NaBH4 | ||
| 653 | |a amino-substituted fused oxazolocoumarin | ||
| 653 | |a fused oxazolocoumarins | ||
| 653 | |a chemoselective reduction | ||
| 653 | |a o-hydroxynitrocoumarins | ||
| 653 | |a benzimidazole | ||
| 653 | |a nucleophilic aromatic substitution | ||
| 653 | |a thiosemicarbazone | ||
| 653 | |a n/a | ||
| 856 | 4 | 0 | |a www.oapen.org |u https://mdpi.com/books/pdfview/book/4510 |7 0 |z Get Fullteks |
| 856 | 4 | 0 | |a www.oapen.org |u https://directory.doabooks.org/handle/20.500.12854/76919 |7 0 |z DOAB: description of the publication |