Synthesis and Studies of Symmetrical DitelluraCalix[6]phyrin(1.1.1.1.1.1)s.

Rare examples of ditellura calix[6]phyrin(1.1.1.

Unravelling the Metal Sensing Activity of a Biologically Relevant Fluorescent Crown Ether: A Unified Experimental and Theoretical Study.

1,4-dihydropyridines (DHPs) are biologically active. 1,4-DHP analogs with appropriate substituents also show characteristic fluorescence activity. Here, for the first time, we report a simple and easy synthesis of a novel fluorescent 1,4- DHP derivative of dibenzo[18]-crown-6 (2), which showed promising sensing ability towards physiologically important metal ions.

Synthesis and Studies of Mono-functionalized Telluradithiasapphyrins and Covalently Linked Porphyrin- Telluradithiasapphyrin Dyads.

A series of mono-functionalized aromatic 22π telluradithiasapphyrins containing functional groups such as p-bromophenyl, p-iodophenyl, p-nitrophenyl and p-trimethylsilylethynyl phenyl groups at one of the meso-positions were synthesized by condensing appropriately functionalized unsymmetrical bithiophene diol and 16-telluratripyrrane in CH Cl under acid-catalyzed conditions. To demonstrate the reactivity of mono-functionalized telluradithiasapphyrins, we synthesized the first examples of covalently linked diphenyl ethyne bridged four novel 18π porphyrin/metalloporphrin-22π telluradithiasapphyrin dyads by coupling meso-ethynyl phenyl porphyrin with telluradithiasapphyrin containing meso-iodophenyl group under Pd(0) coupling conditions followed by metalation of porphyrin unit by treating free base dyad with appropriate metal salts. The dyads were characterized and studied by mass, 1D & 2D NMR, absorption, cyclic voltammetry, fluorescence and DFT techniques.

Vacatadithiasapphyrins: Synthesis, Structure, and Spectral and Redox Properties.

Four examples of novel aromatic [22]vacatadithiasapphyrins were synthesized by refluxing appropriate [22]telluradithiasapphyrins in 1,2-dichlorobenzene in the presence of excess HCl followed by simple column chromatographic purification. The [22]vacatadithiasapphyrins can exist in three conformers "in", "out", and "zigzag" w.r.

Synthesis and Studies of Core-Modified Tellura Dithiasapphyrins.

Four different aromatic -substituted tellurophene-containing dithiasapphyrins were synthesized by acid-catalyzed [3+2] condensation of 16-telluratripyrrane with bithiophene diol in 22-23% yields. The structural, spectral, and electrochemical properties of tellura dithiasapphyrins were studied and compared with those of previously reported aza (pyrrole)- and other heterocycle (furan, thiophene, and selenophene)-containing dithiasapphyrins. Nuclear magnetic resonance studies indicated that the tellurophene ring in tellura dithiasapphyrins is in the normal conformation, facing toward the inner core, but flips in diprotonated derivatives to an inverted conformation, facing away from the macrocyclic core, unlike aza- and other heterocycle-containing dithiasapphyrins in which pyrrole and the corresponding heterocycle ring always prefer to be in inverted conformation in their neutral and protonated forms.

Tellurophene-Containing Core-Modified Pentaphyrin(2.1.1.1.1)s.

Various core-modified tellurophene-containing pentaphyrin(2.1.1.

Copper-Catalyzed Regioselective Synthesis of Multisubstituted Furans by Coupling between Ketones and Aromatic Olefins.

A regioselective synthesis of multisubstituted furan derivatives has been developed via Cu(II)-catalyzed intermolecular annulation of aryl ketones with a wide range of aromatic olefins under ambient air in good yields. This protocol is applicable to both cyclic and acyclic aryl ketones.

Rapid decadal evolution in the groundwater arsenic content of Kolkata, India and its correlation with the practices of her dwellers.

Increasing arsenic contamination in the groundwater is one of the biggest environmental challenges that the Bengal delta is facing today. Groundwater is still the main source of water for a large number of population in this region and therefore, significant presence of toxic arsenic has a direct consequence on human lives here. Moreover, arsenic also enters into the food chain through the consumed agricultural products grown in this area.

Rhodium-Catalyzed Selective Mono- and Diamination of Arenes with Single Directing Site "On Water".

A Rh(III)-catalyzed selective C-H amination of 2-phenylpyridine derivatives is reported. With pyridine as a directing group, the reaction has high mono- or diamination selectivity, and a wide range of effective substrates, including electron-deficient and -rich aryl azides. Water helps to promote C-H activation, and the concept of a water promoted rollover mechanism is postulated for the diamination step.

[RhCp*Cl₂]₂-catalyzed directed N-Boc amidation of arenes "on water".

Rhodium(III) catalysis "on water" is effective for directed C-H amidation of arenes. The catalytic process is promoted by OH groups present on the hydrophobic water surface and is inefficient in all (most) common organic solvents investigated so far. In the presence of easily prepared tert-butyl 2,4-dinitrophenoxycarbamate, a new and stable nitrene source, the "on water" reaction can efficiently provide the desired N-Boc-aminated products with good functional group tolerance.

Copper-mediated synthesis of substituted 2-aryl-N-benzylbenzimidazoles and 2-arylbenzoxazoles via C-H functionalization/C-N/C-O bond formation.

An efficient method for the transformation of N-benzyl bisarylhydrazones and bisaryloxime ethers to functionalized 2-aryl-N-benzylbenzimidazoles and 2-arylbenzoxazoles is described. The protocol involves a copper(II)-mediated cascade C-H functionalization/C-N/C-O bond formation under neutral conditions. Substrates having either electron-donating or -withdrawing substituents undergo the cyclization to afford the target heterocycles at moderate temperature.

Pd-catalyzed C-H activation/C-N bond formation: a new route to 1-aryl-1H-benzotriazoles.

A method for the C-H activation of aryl triazene compounds followed by intramolecular amination is described. It involves the use of a catalytic amount of Pd(OAc)(2) that efficiently effects the cyclization to provide 1-aryl-1H-benzotriazoles at moderate temperature.

Copper(II)-catalyzed conversion of bisaryloxime ethers to 2-arylbenzoxazoles via C-H functionalization/C-N/C-O bonds formation.

A copper(II)-catalyzed conversion of bisaryloxime ethers to 2-arylbenzoxazoles has been developed. The reaction involves a cascade C-H functionalization and C-N/C-O bond formation under oxygen atmosphere.

Cobalt-catalyzed intramolecular C-N and C-O cross-coupling reactions: synthesis of benzimidazoles and benzoxazoles.

Cobalt(ii)-complex catalyzes efficiently the intramolecular C-N and C-O cross-couplings of Z-N'-(2-halophenyl)-N-phenylamidines and N-(2-bromophenyl)benzamides to afford the corresponding substituted benzimidazoles and benzoxazoles in the presence of K(2)CO(3) at moderate temperature. The protocol is general, air stable and affords the products selectively in moderate to high yield.

Ligand-free copper-catalyzed synthesis of substituted benzimidazoles, 2-aminobenzimidazoles, 2-aminobenzothiazoles, and benzoxazoles.

The synthesis of substituted benzimidazoles, 2-aminobenzimidazoles, 2-aminobenzothiazoles, and benzoxazoles is described via intramolecular cyclization of o-bromoaryl derivatives using copper(II) oxide nanoparticles in DMSO under air. The procedure is experimentally simple, general, efficient, and free from addition of external chelating ligands. It is a heterogeneous process and the copper(II) oxide nanoparticles can be recovered and recycled without loss of activity.

Synthesis, structure, and application of self-assembled copper(II) aqua complex by H-bonding for acceleration of the nitroaldol reaction on water.

Simple addition: Copper(II) aqua complex 1 can be prepared in a one-pot synthesis and is self-assembled by H-bond interactions. Complex 1 is shown to accelerate the nitroaldol reaction on water, which is a heterogeneous process, requiring no additive or base, and 1 can be recycled without loss of activity. Copper(II) aqua complex 1 has been prepared in a one-pot synthesis.

A mild and regioselective method for alpha-bromination of beta-keto esters and 1,3-diketones using bromodimethylsulfonium bromide (BDMS).

Bromodimethylsulfonium bromide has been found to be an effective and regioselective reagent for alpha-monobromination of beta-keto esters and 1,3-diketones. A wide variety of beta-keto esters and 1,3-diketones undergo chemoselective alpha-monobromination with excellent yields at 0-5 degrees C or room temperature. The notable advantages of this protocol are no need of chromatographic separation, use of less hazardous reagent than molecular bromine, and no added base, Lewis acid, or other catalyst.