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Journal of Medicinal Chemistry, ISSN 0022-2623, 11/2016, Volume 59, Issue 22, pp. 10147 - 10162
Journal Article
Journal of Medicinal Chemistry, ISSN 0022-2623, 03/2013, Volume 56, Issue 6, pp. 2547 - 2555
Journal Article
4. Phosphorus–nitrogen compounds. Part 42. The comparative syntheses of 2-cis-4-ansa(N/O) and spiro(N/O) cyclotetraphosphazene derivatives: spectroscopic and crystallographic characterization, antituberculosis and cytotoxic activity studies (Electronic supplementary information (ESI) available: Listings of the materials used for syntheses and general physical measurements (Section S1), the antimicrobial activities (Section S2), DNA–compound interactions, and HindIII and BamHI digestions of compound–pBR322 plasmid DNA (Section S3), the determination of the cytotoxic activity with WST assay, and analysis of apoptotic and necrotic cells (Sections S4 and S5), and the determination of antituberculosis activity (Section S6), the experimental HRMS and simulated HRMS spectrum of 3d (Fig. S1), the HMBC and HSQC spectra of 3a (Fig. S2), the shape of the phosphazene ring in 4 with torsion angles given (Fig. S3), the crystal ring conformations (Fig. S4), the OCPA response of a gold electrode including mono-ferrocenylphosphazenes (Fig. S5), the current response validating the 4b compound memory switching for 106 cycles (Fig. S6), the TG curves of the cyclotetraphosphazenes (Fig. S7 and S8), the energy levels of the mono-ferrocenylphosphazene compounds (Table S1), the antimicrobial activities of the cyclotetraphosphazenes expressed as inhibition zones (Table S2), minimum inhibitory and bactericidal concentrations of the compounds against test strains (Table S3), X-ray crystallographic files in CIF format for compound 4. CCDC 1570650 (4). For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c9nj00577c)
New Journal of Chemistry, ISSN 1144-0546, 01/2019, Volume 43, Issue 18, pp. 6856 - 6873
The reaction of N4P4Cl8 (1) with one equimolar amount of the sodium salt of an N/O donor-type bidentate ligand (2) afforded two kinds of derivatives, namely,... 
Gold | Amines | Energy levels | Computer simulation | Shape memory | Sodium salts | Nitrogen compounds | Cytotoxicity | Derivatives | Crystallography | Phosphazene | Antiinfectives and antibacterials | Format | Tuberculosis | Spectrum analysis | Oxidation | NMR spectroscopy | Plasmid DNA | Deoxyribonucleic acid--DNA | Spiro compounds
Journal Article
Chemical Society Reviews, ISSN 0306-0012, 1/2012, Volume 41, Issue 3, pp. 16 - 174
The enantioselective synthesis of spirocycles has been a long time pursued dream for organic chemists. Since the first pioneering efforts of Tamao and... 
PALLADIUM(II) COMPLEXES | DOMINO REACTIONS | RHODIUM(I) COMPLEX | ASYMMETRIC ALDOL REACTIONS | ALLYLIC ALKYLATION | BETA-LACTONES | SPIROCYCLIC OXINDOLES | 2+2+2 CYCLOADDITION | ORGANOCATALYTIC CASCADE REACTIONS | CONCISE SYNTHESIS | CHEMISTRY, MULTIDISCIPLINARY | Construction | Synthesis | Asymmetry | Chemists | Trends | Spiro compounds | Dreams
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 01/2018, Volume 360, Issue 2, pp. 194 - 228
Journal Article
ACS Catalysis, ISSN 2155-5435, 10/2016, Volume 6, Issue 10, pp. 6930 - 6934
An efficient enantioselective insertion of α-diazoesters and α-diazoketones into O–H bonds of carboxylic acids was realized by the use of Rh2(OAc)4 and a... 
insertion | chiral guanidine | asymmetric catalysis | carboxylic acids | rhodium | PALLADIUM | CARBENOIDS | ENANTIOSELECTIVE SYNTHESIS | CHEMISTRY, PHYSICAL | SPIRO PHOSPHORIC-ACIDS | DIAZOCARBONYL COMPOUNDS | CINCHONA ALKALOIDS | CHIRAL ALLENOATES | GUANIDINE | DIAZOKETONES | DERIVATIVES
Journal Article
Chemical Communications, ISSN 1359-7345, 10/2010, Volume 46, Issue 37, pp. 6953 - 6955
The synthesis of Spiro compounds via a Michael-Michael-aldol reaction is reported. The reaction affords spirooxindole derivatives in good yields and in almost... 
ELECTRONIC CIRCULAR-DICHROISM | SPIROCYCLIC OXINDOLES | CHEMISTRY, MULTIDISCIPLINARY | CONSTRUCTION | Cyclization | Stereoisomerism | Spiro Compounds - chemical synthesis | Molecular Structure | Catalysis | Spiro Compounds - chemistry | Aldehydes - chemistry
Journal Article
Journal Article
Advanced Functional Materials, ISSN 1616-301X, 05/2006, Volume 16, Issue 7, pp. 966 - 974
Journal Article
Cancer Letters, ISSN 0304-3835, 2010, Volume 332, Issue 2, pp. 295 - 303
Journal Article