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TABLE OF CONTENTS

Volume 17 Issue 1 , Pages 1 - 79 (January 2003)


Editorial

Editorial: main group metal compounds (p 1)
Peter Craig, Marcel Gielen
Published Online: Dec 6 2002 6:43AM
DOI: 10.1002/aoc.405

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Environment, Biology and Toxicology

Review: Biodegradation of tributyltins (organotins) by marine bacteria (p 3-8)
S.. Dubey, U. Roy
Published Online: Dec 6 2002 6:43AM
DOI: 10.1002/aoc.394

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Organotin(IV) complexes of ethylsarcosine hydrochloride: synthesis, characterization and in vitro cytotoxic activity (p 9-16)
L. Ronconi, C. Marzano, U. Russo, S. Sitran, R. Graziani, D. Fregona
Published Online: Dec 6 2002 6:43AM
DOI: 10.1002/aoc.389

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The cholesterol pathway of Trypanosoma congolense could be a target for triphenyltinsalicylate and triphenylsiliconsalicylate inhibition (p 17-22)
Andrew J. Nok, Ishaya H. Nock, Josiah J. Bonire
Published Online: Dec 6 2002 6:43AM
DOI: 10.1002/aoc.368

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Speciation Analysis

Electrochemically generated tungsten-based active species as catalysts for metathesis-related reactions: 1. Acyclic diene metathesis polymerization of 1,9-decadiene (p 23-27)
Okan Dereli, Bülent Düz, Birgül Zümreogbrevelu-Karan, Yavuz Idotmamogbrevelu
Published Online: Dec 6 2002 6:43AM
DOI: 10.1002/aoc.390

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Materials, Nanoscience and Catalysis

Review: Chemistry of the phosphinophosphinidene tBu2PbondP, a novel pi-electron ligand (p 28-35)
Jolanta Olkowska-Oetzel, Jerzy Pikies
Published Online: Dec 6 2002 6:43AM
DOI: 10.1002/aoc.387

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Synthesis of ruthenium complexes with carbonyl and polypyridyl ligands derived from dipyrido[3,2-a:2prime,3prime-c]phenazine: application to the water gas shift reaction (p 36-41)
P. Aguirre, R. López, D. Villagra, I. Azocar-Guzman, A. J. Pardey, S. A. Moya
Published Online: Dec 6 2002 6:43AM
DOI: 10.1002/aoc.385

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Main Group Metal Compounds

Order-disorder phenomena in crystalline phases of compounds E(XMe3)4 where E = C, Si, Ge and X = Si, Sn (p 42-51)
Xavier Helluy, Angelika Sebald
Published Online: Dec 6 2002 6:43AM
DOI: 10.1002/aoc.382

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tert-Butoxysilanols as model compounds for labileey intermediates of the sol-gel process: crystal and molecular structures of (t-BuO)3SiOH and HO[(t-BuO)2SiO]2H  (p 52-62)
Jens Beckmann, Dainis Dakternieks, Andrew Duthie, Megan L. Larchin, Edward R. T. Tiekink
Published Online: Dec 6 2002 6:43AM
DOI: 10.1002/aoc.380

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Synthesis and characterization of novel chelated dimethylamino lithium alkoxides: molecular structures of [1-LiOC(C6H11)2-2-NMe2C6H4]2 and [1-LiOCPh2CH2-2-NMe2C6H4]2 (p 63-67)
Harbi Tomah Al-Masri, Joachim Sieler, Evamarie Hey-Hawkins
Published Online: Dec 6 2002 6:43AM
DOI: 10.1002/aoc.381

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Synthesis and molecular structure of 2,4,6-tri[bis(diisopropylamino)boryl(methylamino)]borazine, [(NiPr2)2B(Me)N]3B3N3H3 (p 68-72)
Bérangère Toury, David Cornu, Sylvain Lecocq, Philippe Miele
Published Online: Dec 6 2002 6:43AM
DOI: 10.1002/aoc.367

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Crystallographic report: 1,3-Bis[(trimethylsilylmethyl)dichlorostannyl]propane, [(Me3SiCH2)Cl2Sn]2(CH2)3 (p 73)
Dainis Dakternieks, Fong Sheenuan, Andrew Duthie, Edward R. T. Tiekink
Published Online: Dec 6 2002 6:43AM
DOI: 10.1002/aoc.363

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Crystallographic report: 1,4-Bis(triphenylstannylmethyldimethylsilyl)benzene, p-(Ph3SnCH2SiMe2)2C6H4 (p 74)
Dainis Dakternieks, Bernhard Zobel, Edward R. T. Tiekink
Published Online: Dec 6 2002 6:43AM
DOI: 10.1002/aoc.364

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Crystallographic report: 1,4-Bis[(phenyldichlorostannyl)ethyl]benzene, p-(Cl2PhSnCH2CH2)2C6H4 (p 75-76)
Dainis Dakternieks, Andrew Duthie, Edward R. T. Tiekink
Published Online: Dec 6 2002 6:43AM
DOI: 10.1002/aoc.365

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Crystallographic report: 1,4-Bis[bis(trimethylsilyl)methyl-dichlorostannylmethyldimethylsilyl]benzene, p-{[(Me3Si)2CH]Sn(Cl)2CH2SiMe2}2C6H4 (p 77-78)
Dainis Dakternieks, Bernhard Zobel, Edward R. T. Tiekink
Published Online: Dec 6 2002 6:43AM
DOI: 10.1002/aoc.366

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Book Review

Transition metal reagents and catalysts: innovations in organic synthesis. Edited by Jiro Tsuji. John Wiley & Sons, Ltd, Chichester, 2002, xv + 477 pp; price £60.00, euro 99.00. ISBN 0-471-56027-8 (p 79)
Liam R. Cox
Published Online: Dec 6 2002 6:43AM
DOI: 10.1002/aoc.388

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