One pot three component synthesis of spiro [indolo-3,10’-indeno[1,2-b]quinolin]-2,4,11’-triones as a new class of antifungal and antimicrobial agents

A simple and efficient three component procedure has been developed for the synthesis of highly substituted spiro[indolo-3,10'-indeno[1,2-b]quinolin]-2,4,11'-triones by one pot three component condensation of enaminones, isatin and indane-1,3-dione in ethanol:water (1:1) in presence of ceric ammonium nitrate (CAN) as catalyst. This method provides several advantages such as lesser reaction time, high yield of products and operational simplicity. The antimicrobial activity of some of the compounds has been investigated against six microbial strains, some of the tested compounds showed good antimicrobial activity.     

Baseline assessment of doses and risk due to natural radionuclides in edible biota of Domiasiat,Meghalaya, India

Radiation dose-risk assessment was carried out for cereal species Brassica compestris var. dichotoma, Oryza sativa var. Shalum1, Zea mays, Lactuca indica, Cumunis sativum, and Clocasia esculanta due to naturally available radionuclides ⁴⁰K, ²³⁸U and ²³²Th in Domiasiat area. The activity in biota and corresponding soil was measured by precipitation method using NaI(TI) detector. Transfer factor (TF) was for Oryza spp. (1.00E−01-⁴⁰K, 8.76E−05-²³²Th, and 9.11E−05-²³⁸U), for Brassica spp. (5.39E−01-⁴⁰K, 8.17E−04-²³²Th and 2.96E−04-²³⁸U) and for Zea spp. (3.41E−01-⁴⁰K, 5.84E−05-²³²Th, 8.87E−05-²³⁸U) etc., respectively. A detailed physio-morphological study of the biota and extensive investigation of ecosystem was carried out for assessment. The data was modeled using FASSET for dose estimation and obtained total dose was 1.58E−04  \upmu Gy h^-1 \upmu \hbox{Gy}\,h^{-1} in Oryza spp., 2.87E−04  \upmu Gy h^-1 \upmu \hbox{Gy}\,h^{-1} Brassica spp. and 6.90E−03  \upmu Gy h^-1 \upmu \hbox{Gy}\,h^{-1} in Zea spp. etc. The dose was compared with the UNSCEAR dataset for screening level dose for biota. Zea spp. was more susceptible for the chronic radiation exposure.     

New approximate analytical expressions for transient concentration profiles and current pertaining to a homogeneous chemical reaction at hemispherical microelectrodes

A mathematical model corresponding to homogeneous chemical reactions under transient chronoamperometry conditions at hemispherical microelectrodes has been developed. The analytical solutions for the concentration of species and current were obtained using Duhamel's theorem. This closed-form theoretical expression pertains to the transient concentration profiles and fluxes of chemical species involved in chemical and electrochemical reactions at hemispherical microelectrodes. As t → ∞, the analytical expressions corresponding to the concentration and current approach steady-state values. The solutions obtained are explicit only under limiting current conditions. The approximate expressions for concentrations and current as functions of time corresponding to the EC' and CE mechanisms at hemispherical microelectrodes are also reported.     

An efficient one-pot synthesis of carbazates and dithiocarbazates through the corresponding alcohols using Mitsunobu��s reagent

A novel Mitsunobu-based protocol has been developed for the synthesis of carbazates and dithiocarbazates through the variety of corresponding primary, secondary and tertiary alcohols and various kinds of substituted hydrazines using Mitsunobu??s reagent and CO₂/CS₂ system, in good to excellent yields.     

Liquid-chromatographic separation and determination of process-related impurities, including a regio-specific isomer of celecoxib on reversed-phase C18 column dynamically coated with hexamethyldisilazane.

A simple and rapid reversed-phase high-performance liquid-chromatographic method for the separation and determination of process-related impurities of celecoxib (CXB) in bulk drugs and pharmaceuticals was developed. The separation of impurities viz., 4-methylacetophenone (I), 1-(4-methylphenyl)-4,4,4-trifluorobutane-1,3-dione (II), 4-hydrazinobenzene sulfonamide (III) and a regio-specific isomer [3-(4-methylphenyl)-5-trifluoromethyl-1H-pyrazole-1-yl]-benzenesulfonamide (IV), was accomplished on an Inertsil ODS-3 column dynamically coated with 0.1% hexamethyldisilazane (HMDS) in acetonitrile:water (55:45 v/v) as a mobile phase and detection at 242 nm using PDA at ambient temperature. The chromatographic conditions were optimized by studying the effects of HMDS, an organic modifier, time of silanization and column temperature. The method was validated and found to be suitable not only for monitoring the synthetic reactions, but also to evaluate the quality of CXB.     

An Efficient, One-Pot, Triton-B Catalyzed Synthesis of O -Alkyl- S -methyl Dithiocarbonates

A novel process for the one-step conversion of a variety of primary and secondary alcohols into their O-alkyl-S-methyl dithiocarbonates using methyl iodide catalyzed by the Triton-B/CS₂ system was developed. Thus, O-alkyl-S-methyl dithiocarbonates were obtained in very good to excellent yields. This protocol is mild and efficient compared to other methods.     

Die Kinetik der Entladung von Thorium (IV) in Gegenwart von Äthylen-bis(3-mercaptopropionat) an der Quecksilbertropfelektrode

The reduction of thorium at the dropping mercury electrode in presence of ethylene bis(3-mercaptopropionate) has been found to be irreversible and kinetically controlled. The kinetics of the electrode reaction has been investigated adopting the treatment followed byKoutecky.

---

---

Mit 1 Abbildung     

Studies on binuclear Schiff base derivatives having a Si?O?Sb (V) linkage

Schiff base derivatives of the type Ph₃Si? O? Sb(NO)Ph₃ (where NO represents the donor system of a monobasic bidentate ligand) have been synthesized. These are obtained as coloured solids; they are non-electrolytes and monomeric in nature, and have been characterized by elemental analysis, IR and ¹H NMR. Spectral studies suggest that silicon and antimony atoms are in tetra- and hexa-coordinated states, respectively.     

Triton-B Catalyzed Efficient One-Pot Synthesis of Dithiocarbamate Esters

A novel process for the one-step chemoselective conversion of alkyl halides into dithiocarbamates as protected amines was developed using benzyltrimethylammonium hydroxide (Triton-B) in presence of carbon disulfide. Thus, dithiocarbamates of different amines were prepared in very good to excellent yields. This protocol is mild, chemoselective, and efficient compared to other methods.