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Keyword Connections - cyclization Keywords

Connection Type	Connection
Journals	Dalton transactions (Cambridge, England : 2003) Chemistry, an Asian journal current computer-aided drug design Chemical science
Research Groups	No Research Group Connected
Bibliographies	[1] One-Pot Cascade Transformation of Glucal into Structurally Diverse Drug-Like Scaffolds. [2] Synthesis and structural characterization of 20-membered macrocyclic rings bearing trans-chelating bis(N-heterocyclic carbene) ligands and the catalytic activity of their palladium(ii) complexes. [3] Two non-identical twins in one unit cell: characterization of 34π aromatic core-modified octaphyrins, their structural isomers and anion bound complexes. [4] Synthesis, Antibacterial Activity and Molecular Docking of Phospholidinones in Stigmastane Series. [5] syntheses of non-aromatic medium and large rings synthesized via phenylnitrenium ions [6] crystal structure of 5-[4-(dimethylamino)phenyl]-3-(4-methylphenyl)-4,5-dihydro-1h-pyrazole-1-carbaldehyde [7] oxidative radical cyclization–cyclization reaction leading to 1h-benzo[f]isoindole derivatives [8] synthesis and characterization of a novel series of meso (nitrophenyl) and meso (carboxyphenyl) substituted porphyrins [9] mgo nanoparticles: an efficient, green and reusable catalyst for the one- pot syntheses of 2,6-dicyanoanilines and 1,3-diarylpropyl malononitriles under different conditions [10] dihydrodipyridopyrazines: synthesis and functionalization [11] The hetero-Friedel-Crafts-Bradsher Cyclizations with Formation of Ring Carbon-Heteroatom (P, S) Bonds, Leading to Organic Functional Materials [12] 5-Unsubstituted pyrido[3,2,1-jk]carbazol-6-ones: Syntheses, substitution, and cyclization reactions [13] Facile synthesis of 5H-benzo[b]carbazol-6-yl ketones via sequential reaction of Cu-catalyzed Friedel-Crafts alkylation, iodine-promoted cyclization, nucleophilic substitution and aromatization [14] Characterization of Thermostable and Chimeric Enzymes via Isopeptide Bond-Mediated Molecular Cyclization. [15] Synthesis of Flavones by Thallium(III) p-tosylate-catalyzed Regioselective Cyclization of o-(Alkynon-1-yl)phenols [16] Divergent synthesis of flavones and aurones via base-controlled regioselective palladium catalyzed carbonylative cyclization [17] A simple and efficient synthesis of 3,4,5-trisubstituted/N-fused 1,2,4-triazoles via ceric ammonium nitrate catalyzed oxidative cyclization of amidrazones with aldehydes using polyethylene glycol as a recyclable reaction medium [18] Cyclization of 2-azido-3-(alkyl-N-nitrosoamino)-1,4-naphthoquinones to 1-alkyl-1H-naphtho[2,3-d][1,2,3]triazole-4,9-dione 2-oxides [19] Intramolecular cyclization of 1,2-bis(N-alkoxy-N-nitrosoamino)alkanes: A unique route to 4,5-dihydro-1,2,3-triazole 2-oxides [20] A convenient synthesis of 2-dialkylamino-1,3-oxathiol-2-ylium salts by an unusual cyclization of 2-oxoalkyl dithiocarbamates [21] Correction: Highly Regioselective Synthesis of Oxindolyl-Pyrroles and Quinolines via a One-Pot, Sequential Meyer-Schuster Rearrangement, Anti-Michael Addition/C(sp<sup>3</sup>)-H Functionalization, and Azacyclization(ACS Omega (2018) 3:3 (2934-2946) DOI: 10.1021/acsomega.8b00147) [22] DFT/TDDFT, NPA, and AIM-based study of the molecular switching properties of photocyclization and metallochromism of the DAE complexes [23] Antifungal activity and tautomeric cyclization equilibria of formylphenylboronic acids. [24] Application of Thiol-yne/Thiol-ene Reactions for Peptide and Protein Macrocyclizations. [25] Visible Light-Promoted Cascade Radical Cyclization: Synthesis of 1,4-Diketones Containing Chroman-4-One Skeletons. [26] Photoinduced synthesis of fluorinated dibenz[b,e]azepines via radical triggered cyclization. [27] Eosin Y-catalyzed visible-light-mediated aerobic oxidative cyclization of N,N-dimethylanilines with maleimides [28] Optimizing ligand structure for low-loading and fast catalysis for alkynyl-alcohol and -amine cyclization. [29] Isolation of ruthenium-indoline and -indole zwitterion complexes: Insight into the metal-induced cyclization of aniline-tethered alkynes and strategy to lower the activation barrier of metal-vinylidene formation [30] Catalyst-free [4 + 2] cyclization of para-quinone methide derivatives with homophthalic anhydrides. [31] Highly Chemo- and Diastereoselective Construction of Quaternary Stereocenters through Palladium-Catalyzed [3 + 2] Cyclization of 5-Alkenyl Thiazolones. [32] Intramolecular oxidative cyclization of N-(2,2,2-trifluoro-1-(phenylimino)ethyl)benzimidamide. [33] Cyclization of Thiopropargyl Benzimidazoles by Combining Iron(III) Chloride and Diorganyl Diselenides. [34] Study of the Chemoselectivity of Multicomponent Heterocyclizations Involving 3-Amino-1,2,4-triazole and Pyruvic Acids as Key Reagents, and Biological Activity of the Reaction Products [35] Access to 1,2,3-triazole-fused isoindolines via an unexpected Lewis acid catalyzed cyclization reaction [36] Combined XRD and DFT studies towards understanding the impact of intramolecular H-bonding on the reductive cyclization process in pyrazole derivatives [37] Bifunctional Squaramide-Catalyzed Asymmetric [3 + 2] Cyclization of 2-(1-Methyl-2-oxoindolin-3-yl)malononitriles with Unsaturated Pyrazolones To Construct Spirooxindole-Fused Spiropyrazolones. [38] A Formal Total Synthesis of (±)-Kopsihainanine A Using a Raney-Cobalt Mediated Reductive Cyclization Route to Polyhydroquinolines. [39] Sesquiterpene Cyclizations inside the Hexameric Resorcinarene Capsule: Total Synthesis of δ-Selinene and Mechanistic Studies. [40] B(CF)-catalyzed dehydrogenative cyclization of -tosylhydrazones and anilines a Lewis adduct: a combined experimental and computational investigation. [41] Nanoporous Cu doped ZnS nanoparticles an efficient photo catalyst for the chemoselective synthesis of 2-substituted azoles via C-N arylation/ CSp<inf>3</inf>– H oxidation/ cyclization/dehydration sequence in visible light [42] Improving the aqueous solubility of HCV-E2 glycoprotein epitope mimics by cyclization using POLAR hinges. [43] Phosphazene Superbase-Mediated Regio- and Stereoselective Iodoaminocyclization of 2-(1-Alkynyl)benzamides for the Synthesis of Isoindolin-1-ones. [44] Synthesis of 1,3-oxaphospholes via chromium mediated cyclization of carbenes, carbon monoxide, and phospha-alkynes [45] Synthesis of 1,3-oxaphospholes via chromium mediated cyclization of carbenes, carbon monoxide, and phospha-alkynes [46] Palladium-catalyzed regioselective aerobic oxidative cyclization via C-H activation in chloroquine analogues: Synthesis and cytotoxic study [47] Sustainable and recyclable heterogenous palladium catalysts from rice husk-derived biosilicates for Suzuki-Miyaura cross-couplings, aerobic oxidations and stereoselective cascade carbocyclizations [48] A convenient one-pot synthesis of N-fused 1,2,4-triazoles via oxidative cyclization using chromium (VI) oxide [49] Dehydrocyclization of o-Ethyl-, o-Allyl- and o-Isopropylphenols [50] Samarium(II)-iodide-mediated cyclizations in natural product synthesis [51] syntheses of 4-indolylquinoline derivatives via reductive cyclization of indolylnitrochalcone derivatives by fe/hcl [52] reaction mechanism for the cyclization of 3-[ÃŽÂ³,ÃŽÂ³-dimethylallyl]coumaric acid methyl ester in dimethyl sulfoxide (dmso) [53] condensation reactions of 3-oxo-2-arylhydrazonopropanals with active methylene reagents: formation of 2-hydroxy- and 2-amino-6-substituted-5-arylazonicotinates and pyrido[3,2-c]cinnolines via 6π-electrocyclization reactions [54] eosin y catalyzed visible-light-promoted aerobic oxidative cyclization of 2-aminobenzothiazole [55] heterocyclization reactions study of 3-thio and 3-thio-4-amino derivatives of 1,2,4–triazole [56] oxidative radical cyclization–cyclization reaction leading to 1h-benzo[f]isoindole derivatives [57] 2,2′-Biphenol/B(OH)<inf>3</inf> catalyst system for Nazarov cyclization [58] Electrochemical Synthesis of Benzimidazoles via Dehydrogenative Cyclization of Amidines [59] Transition-metal-free synthesis of imidazo[2,1-b]thiazoles and thiazolo[3,2-a]benzimidazoles via an S-propargylation/5-exo-dig cyclization/isomerization sequence using propargyl tosylates as substrates. [60] The hetero-Friedel-Crafts-Bradsher Cyclizations with Formation of Ring Carbon-Heteroatom (P, S) Bonds, Leading to Organic Functional Materials [61] Novel 3,4-dihydro-1,4-oxazine (dehydromorpholine) sulfonamides and sulfones conveniently accessed from suitable a-diazoketones via O[sbnd]H carbene insertion – Cyclization sequence [62] Facile synthesis of 1,4-oxazines by ruthenium-catalyzed tandem N-H insertion/cyclization of α-arylamino ketones and diazo pyruvates [63] Synthesis of dihydrobenzo[1,4]oxazines by palladium-catalyzed cyclization of n-substituted 2-aminophenols with propargylic carbonates [64] One-Pot Synthesis of Enantiopure Spiro[3,4-dihydrobenzo[][1,4]oxazine-2,3'-oxindole] via Regio- and Stereoselective Tandem Ring Opening/Cyclization of Spiroaziridine Oxindoles with Bromophenols. [65] Backbone cyclization of Salmonella typhimurium diaminopropionate ammonia-lyase to enhance the activity and stability. [66] Asymmetric macrocyclization enabled by Rh(III)-catalyzed C[sbnd]H activation: Enantioenriched macrocyclic inhibitor of Zika virus infection