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1.
A. C. Bhasikuttan A. V. Sapre L. V. Shastri 《Journal of photochemistry and photobiology. A, Chemistry》1995,90(2-3):177-182
The reactions of two triphenyl methane (TPM) dyes—crystal violet (CV+) and malachite green (MG+)—with N3• and OH• radicals were studied by pulse radiolytic kinetic spectrophotometry. The rate constants for the reaction of the cationic dyes (D+) with N3• are (9.0±0.6)×109 and (3.0±0.2)×109 dm3 mol−1 s−1 respectively and those for the reaction with OH• are obtained as (8.0±0.6)×109 and (1.1±0.1)×109 dm3 mol−1 s−1 respectively. The transient spectra resulting from the oxidation of the dyes were characterized. The time-resolved spectra indicate that the reaction with OH• radicals initially generates an adduct which subsequently dissociates to form the radical dication D•2+. The D•2+ species decay by further reaction with the parent dye. 相似文献
2.
A stereoselective conversion of the readily available (+)-car-3-ene into (+)-carvone by two different routes is described. This is the first report on synthesis of carvone from car-3-ene. 相似文献
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Abstract On radiolysis tris(acetylacetonato) cobalt(III) in aqueous solutions is found to get reduced by reaction with (1) hydrated electrons, (2) H atoms, (3) OH radicals and (4) C2H2OH radicals. The bimolecular rate constants for the first three reactions, determined by competition kinetics are: 4 × 1010, 2.3 × 109 and 4.7 × 109 M?1sec?1 respectively. Absorption spectra of the irradiated solutions indicate the formation of bis(acetylacetonato) cobalt(II) from reaction (1), but not from (3). The total cobaltous yield in air-free solutions is given byG(Co++) = 5.6 and 6.5 at pH 6.5 and 1 respectively. It appears that Geaq- ∽ H + GoH ∽ 2.8 in neutral solutions. Considerations of material balance for the primary yields of radiolysis of water suggest the possibility that the so-called independent H-atoms in neutral solutions are probably excited water molecules or ion-pairs. 相似文献
5.
Jyoti M. Madar Samundeeswari L. Shastri Megharaja Holiyachi Nirmala Naik Rashmi Kulkarni 《合成通讯》2018,48(4):375-386
Pursuing our recent interest regarding antimicrobial and anti-inflammatory activities of coumarin derivatives, we have synthesized a series of coumarin-linked pyridopyrimidinones by using Baylis Hillman adduct in aqueous condition with high purity. Pyrido[1,2-a]pyrimidin-2-ones are important class of heterocyclic compounds because of their use in medicinal and agro chemistry as active agents. All these newly synthesized compounds were evaluated for their antimicrobial and anti-inflammatory activity. Coumarin pyridopyrimidinones showed excellent anti-inflammatory activity against both MMP-2 and MMP-9 gelatinase zymography, whereas considerable good activity against Gram-positive and Gram-negative bacterial strains; however, antifungal activity observed in these series is more or less inactive. The active compounds of these series would be promising structural templates for the development of novel and more efficient anti-inflammatory agent. 相似文献
6.
K. Shivashankar Manohar V. Kulkarni Lokesh A. Shastri Vijaykumar P. Rasal Sandur V. Rajendra 《Phosphorus, sulfur, and silicon and the related elements》2013,188(9):2187-2200
Various 4-aryloxymethylcoumarins have been obtained by the r.t. allylic substitution with formylphenols. These have been further reacted with o-aminothiophenol resulting in the formation of a benzothiazole skeleton. These compounds have been synthesised with a view to study their potential as microbial growth inhibitors. Comparative studies on the spectral and antimicrobial activities have also been carried out. 相似文献
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The first efficient transformation of 4-bromomethylcoumarins and 4-bromomethylcarbostyrils to 4-formylcoumarins and 4-formylcarbostyril under aqueous conditions has been achieved by modifying the Kornblum method, resulting in excellent yield. The experimental method is very simple and economical; no further purification is required and the experimental conditions have been optimized. All the isolated compounds were characterized by infrared, NMR, and mass spectroscopy, and some of the compounds have been analyzed by single-crystal x-ray analysis. 相似文献
8.
An attempted reaction of 4‐bromomethylcoumarin with 2‐hydroxy aromatic aldehyde/2‐hydroxy aromatic ketone at room temperature in the presence of a mild base resulted in the formation of cis‐2′,3′‐dihydro‐3‐hydroxybenzofuranylcoumarins by carbanion addition across the carbonyl carbon. 相似文献
9.
Lokesh A. Shastri Suresh Kumar Kailasa Hui‐Fen Wu 《Rapid communications in mass spectrometry : RCM》2009,23(15):2247-2252
Fluorescent semiconductor quantum dots (QDs) exhibit great potential and capability for many biological and biochemical applications. We report a simple strategy for the synthesis of aqueous stable ZnSe QDs by using cysteine as the capping agent (ZnSe‐Cys QDs). The ZnSe QDs can act as affinity probes to enrich peptides and proteins via direct matrix‐assisted laser desorption/ionization time‐of‐flight mass spectrometry (MALDI‐TOFMS) analysis. This nanoprobe could significantly enhance protein signals (insulin, ubiquitin, cytochrome c, myoglobin and lysozyme) in MALDI‐TOFMS by 2.5–12 times compared with the traditional method. Additionally, the ZnSe‐Cys QDs can be applied as heat absorbers (as accelerating probes) to speed up microwave‐assisted enzymatic digestion reactions and also as affinity probes to enrich lysozyme‐digested products in MALDI‐TOFMS. Furthermore, after the enrichment experiments, the solutions of ZnSe‐Cys QDs mixed with proteins can be directly deposited onto the MALDI plates for rapid analysis. This approach shows a simple, rapid, efficient and straightforward method for direct analysis of proteins or peptides by MALDI‐TOFMS without the requirement for further time‐consuming separation processes, tedious washing steps or laborious purification procedures. The present study has demonstrated that ZnSe‐Cys QDs are reliable and potential materials for rapid, selective separation and enrichment of proteins as well as accelerating probes for microwave‐digested reactions for proteins than the regular MALDI‐MS tools. Additionally, we also believe that this work may also inspire investigations for applications of QDs in the field of MALDI‐MS for proteomics. Copyright © 2009 John Wiley & Sons, Ltd. 相似文献
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