radiation chemistry of indole and its derivatives.

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University of Salford , Salford
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Organic Chemistry, Volume The Chemistry of Indoles discusses the chemistry of indole derivatives. This book explores the potent biological activity of several indole derivatives and explains the structure of indole alkaloids.

Organized into 10 chapters, this monograph starts with an overview of the most important types of reactions of the Book Edition: 1. 2,2-Bis-(3-indoly)indol-3(2)-one and polymer are the major products derived by -irradiation of aqueous solutions of indole in argon, nitrous oxide, and oxygen.

Small amounts of indoxyl, indoxyl red, indigo, and indirubin are also formed. Anthranilic acid appears to be produced in oxygen. A reaction pathway is discu. Research has been driven by the wide range of indole derivatives which occur in nature and through the biological activity of many indole derivatives, of both natural and synthetic book provides a systematic guide to the most useful and important reactions in the field for both synthesis and synthetic modification of the indole : $ This book is radiation chemistry of indole and its derivatives.

book of 12 chapters that specifically cover the chemistry of the complex indoles. The introductory chapters deal with the origin, isolation, characterization, basic chemistry, and simple derivatives of indole alkaloids. The remaining chapters examine the biogenesis, basic chemistry, stereochemistry, and structure of selected.

Various methodologies for the synthesis of indole and its derivatives in water are described. Different elements ranging from p-block elements, transition metals to.

indole induces spore formation in the myxobacterium, Stigmatella aurantiaca Spore formation of S. aurantiaca is not strictly coupled to fruiting body formation and can be directly induced in liquid culture by a number of chemicals.

Of which the most potent are indole and some of its derivatives. During. Read the latest chapters of Organic Chemistry atElsevier’s leading platform of peer-reviewed scholarly literature Book chapter Full text access VI - Rearrangement, Ring Expansion, and Ring Opening Reactions of Indoles Naturally Occurring Derivatives of Indole and Indoles of Physiological and Medicinal Significance.

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The valence radiation chemistry of indole and its derivatives. book core-level photoelectron spectra of gaseous indole, 2,3-dihydroazaindole, and 3-formylindole have been investigated using VUV and soft X-ray radiation supported by both an ab initio electron propagator and density functional theory calculations.

Three methods were used to calculate the outer valence band photoemission spectra: outer valence Green function, partial third.

Indole heterocyclic molecules have huge significance in the field of medicinal chemistry. • The present review focus on synthetic medicinal chemistry, SAR and pharmacological significance of indole derivatives.

Description radiation chemistry of indole and its derivatives. PDF

• Clinical and preclinical indole derivatives and. Several researchers from various Indian universities and national laboratories use the PULAF and some of the projects that are currently undertaken by our group and others include the radiation chemistry of indole and chalcone derivatives, herbal antioxidants, structure-reactivity studies in cinnamates, redox chemistry of inorganic metal.

Various methodologies for the synthesis of indole and its derivatives in water are described. Different elements ranging from p-block elements, transition metals to lanthanides, along with peptides, surfactants, ionic liquids, and nanoparticles have been used to synthesize either the indole nucleus or its reactions are conducted both in water only and in a mixture of water.

The interaction of indole, imidazole, and their derivatives with α-hydroxyethyl radicals has been studied by the radiation and peroxide initiation of free-radical processes. The enthalpies of H-atom addition to the multiple bonds of the test compounds, which characterize their oxidation properties, have been calculated within the framework of the density functional theory.

A very mild method for the introduction of functionalized alkylselenyl group at C‐3 position of the indole ring was developed. The proposed procedure consists of an electrophilic substitution of indole and its derivatives with bis(O,O‐diisopropoxyphosphorothioyl) diselenide and subsequent cleavage of the P–Se bond with tetrabutylammonium fluoride in the presence of various electrophilic.

Title:Recent Developments in the Synthesis and Antimicrobial Activity of Indole and its Derivatives VOLUME: 16 ISSUE: 1 Author(s):Jaskirat Kaur, Divya Utreja*, Ekta, Nisha Jain and Shivali Sharma Affiliation:Department of Chemistry, Punjab Agricultural University, LudhianaDepartment of Chemistry, Punjab Agricultural University, LudhianaDepartment of Chemistry, Punjab.

The structures of radiation-induced radicals generated from indole and a selected number of its derivatives in methanolic glasses at 77 K have been investigated by e.s.r. spectroscopy. From the spectral characteristics [tt, (2)and (2) G for indole].

Indole derivatives are recognized to prevent proliferation and invasion of many cancer cells. Conclusion: This review presents the existing status and the very recent studies of indoles which have promising activities such as derivatives of indolecarbinol, 3,3'-diindolylmethane (DIM), isatin etc.

Radiation Chemistry of Aqueous Solutions of Indole and its Derivatives by B Iddon, GO Phillips, KE Robbins, JV Davies (University of Salford, ) Radiation Sterilization of Pharmaceuticals and Biomedical Products by R Blackburn, B Iddon, JS Moore, GO Phillips, DM Power, TW Woodward (International Atomic Energy Agency, Vienna, ).

The reactions of oxidizing radicals (• OH, Br 2 •−, and SO 4 •−) with −OH- −CH 3- or −NH 2-substituted indole chalcones and hydroxy benzenoid chalcones were studied by radiation and quantum chemical • OH radical was found to react by addition at diffusion-controlled rates (k = − × 10 10 dm 3 mol −1 s −1), but Br 2 •− radical reacted by 2 orders.

Indole derivatives are obtained as single regioisomers in high yields. Kaspar, L. Ackermann, Tetrahedron,61, A Pd-catalyzed cascade process consisting of isocyanide insertion and benzylic C(sp 3)-H activation allows the construction of the indole skeleton.

About this Book series The Chemistry of Heterocyclic Compounds, since its inception, has been recognized as a cornerstone of heterocyclic chemistry.

Each volume attempts to discuss all aspects – properties, synthesis, reactions, physiological and industrial significance – of a specific ring system. Isatin (1H-indole-2,3-dione) and its derivatives represent an important class of heterocyclic compounds that can be used as precursors for drug its discovery, a lot of research work has been done regarding the synthesis, chemical properties, and biological and industrial applications of isatin.

Hai-Lei Cui, Si-Wei Liu, Xue Xiao, Synthesis of Tetrahydroindolizino[8,7- b ]indole Derivatives in the Presence of Fe(OTf) 3 or CF 3 SO 3 H through Intramolecular Dearomatization of Indole, The Journal of Organic Chemistry, /0c, ().

Spectral, Kinetics, and Theoretical Studies of Radical Cations Derived from Thioanisole and Its Carboxylic Derivative. The Journal of Physical Chemistry A(40) Effect of charge scavengers on the radiation-chemical carboxylation of the indole—serine system.

High Energy Radiation Physics and Chemistry ()20 (2. Department of Chemistry, University of Southern Mississippi, Hattiesburg. MSUSA (Received 11 August ; accepred 14 October ) Abstract-The photophysics and photochemistry of tryptophan and its simple derivatives is comprehensively reviewed with special emphasis on excitation by near-UV radiation.

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Topics explicitly. IV.—Syntheses in the indole series. Part II. 5: 6-Benzcarboline and its derivatives. Indole is a well-known privileged structure scaffold occurring in numerous natural products such as alkaloids, peptides and various synthetic compounds.

Because of its biodynamic properties; Indole as well as its derivatives has occupied a unique platform in nitrogen heterocyclic chemistry [1, 2].It is a hetero-atomic planar.

A new series of CB1 ligands with high binding affinity (Ki = − nM) and moderate lipophilicity (cLogD) in the range of − has been synthesized. A structure−activity relationship study demonstrated that for the studied set of aminoalkylindoles, the molecular dipole of the ground state conformation within the series was inversely related to the affinity.

The racemic ligand. Title:IndoleCarbinol (I3C) and its Major Derivatives: Their Pharmacokinetics and Important Roles in Hepatic Protection VOLUME: 17 ISSUE: 4 Author(s):Si-qi Wang, Li-sha Cheng, Yun Liu, Ji-yao Wang and Wei Jiang Affiliation:Department of Gastroenterology, Zhongshan Hospital, Fudan University, Fenglin Road, ShanghaiChina.

Thiazinanes and its isomeric forms represent one of the most important heterocyclic compounds, and their derivatives represented a highly potent drug in disease treatment such as, 1,1-dioxido-1,2-thiazinan-1,6-naphthyridine, which has been shown to have anti-HIV activity by a mechanism that should work as anti-AIDS treatment, while (Z)-methyl 3-(naphthalenylimino)- 2-thiaazaspiro[5 5.

The interaction of indole, imidazole, and their derivatives with α-hydroxyethyl radicals has been studied by the radiation and peroxide initiation of free-radical processes.

Molecular Shape. The linkage between indoles B and C was examined as a means of changing the overall shape of the molecule. Rings B and C in 1a are linked through the 6–6′ carbons. Compounds with 5–6′ (6o), 6–5′ (6p), and 5–5′ (6q) linkages were synthesized and activity data indicated that all three compounds had reduced activity compared to 1a, not only in.Indole derivatives constitute an important class of therapeutical agents in medicinal chemistry including anticancer, antioxidant, antirheumatoidal, aldose reductase inhibitor, and anti-HIV agents.

Reactive oxygen species are constantly generated in the human body and are involved in various physiologically important biological reactions.The first asymmetric synthesis of (S)-Phaitanthrin A and its derivatives via a catalytic aldol reaction of Tryptanthrin and ketones is described, in which the cheap, easily prepared natural amino acid salts exhibited unique catalytic ability; importantly, this methodology tolerates a range of substrates with different substitution patterns.