@article {1489,
	title = {Crystal structures of protein phosphatase-1 bound to motuporin and dihydromicrocystin-LA: Elucidation of the mechanism of enzyme inhibition by cyanobacterial toxins},
	journal = {Journal of Molecular Biology},
	volume = {356},
	number = {1},
	year = {2006},
	note = {ISI Document Delivery No.: 007AFTimes Cited: 17Cited Reference Count: 42},
	month = {Feb},
	pages = {111-120},
	type = {Article},
	abstract = {The microcystins and nodularins are tumour promoting hepatotoxins that are responsible for global adverse human health effects and wildlife fatalities in countries where drinking water supplies contain cyanobacteria. The toxins function by inhibiting broad specificity Ser/Thr protein phosphatases in the host cells, thereby disrupting signal transduction pathways. A previous crystal structure of a microcystin bound to the catalytic subunit of protein phosphatase-1 (PP-1c) showed distinct changes in the active site region when compared with protein phosphatase-1 structures bound to other toxins. We have elucidated the crystal structures of the cyanotoxins, motuporin (nodularin-V) and dihydromicrocystin-LA bound to human protein phosphatase-1c (gamma isoform). The atomic structures of these complexes reveal the structural basis for inhibition of protein phosphatases by these toxins. Comparisons of the structures of the cyanobacterial toxin:phosphatase complexes explain the biochemical mechanism by which microcystins but not nodularins permanently modify their protein phosphatase targets by covalent addition to an active site cysteine residue. (c) 2005 Elsevier Ltd. All rights reserved.},
	keywords = {CATALYTIC SUBUNIT, COMPLEX, crystal structure, cyanobacteria, IN-VIVO, microcystin, MICROCYSTIN-LR, MOLECULAR-MECHANISMS, nodularin, POTENT, PROGRAM, TUMOR-PROMOTER, TYPE-1},
	isbn = {0022-2836},
	url = {<Go to ISI>://000234938600010},
	author = {Maynes, J. T. and Luu, H. A. and Cherney, M. M. and Andersen, R. J. and Williams, D. and Holmes, C. F. B. and James, M. N. G.}
}
@article {1272,
	title = {A convenient way of making arsoxanes (RAsO)(n), X-ray crystal structure of (m-F3CC6H4AsO)(4)},
	journal = {Applied Organometallic Chemistry},
	volume = {19},
	number = {1},
	year = {2005},
	note = {ISI Document Delivery No.: 893NZTimes Cited: 2Cited Reference Count: 22},
	month = {Jan},
	pages = {129-131},
	type = {Article},
	abstract = {The reactions of RLi (R = t-Bu, m-F3CC6H4) with bis(dimethylamino)chloroarsine in diethyl ether at room temperature result in the formation of t-butyl-bis(dimethylamino)arsine (1) and m-trifluoromethylphenyl-bis(dimethylamino)arsine (2). Compounds 1 and 2 were hydrolysed in water solution in the presence of sodium carbonate to give the oxides (t-BuAsO)(n) (3) and (m-F3CC6H4AsO)(n) (4) respectively. The X-ray crystal structure of 4 shows the molecule to be cyclotetrameric with pyramidal arsenic. Copyright (C) 2004 John Wiley Sons, Ltd.},
	keywords = {ALKYLCYCLOARSOXANES, arsenic, ARSINE, arsine oxide, crystal structure, m-trifluromethylphenylarsine oxide, m-trifluromethylphenylarsoxane, NMR, RING, t-butylarsarsoxane, t-butylarsine oxide},
	isbn = {0268-2605},
	url = {<Go to ISI>://000226727800024},
	author = {Sun, H. S. and Patrick, B. O. and Cullen, W. R.}
}
@article {1145,
	title = {Discrimination in the solid-state photodimerization of 1-methyl-5,6-diphenylpyrazin-2-one},
	journal = {European Journal of Organic Chemistry},
	number = {5},
	year = {2005},
	note = {ISI Document Delivery No.: 903LHTimes Cited: 5Cited Reference Count: 18},
	month = {Feb},
	pages = {847-853},
	type = {Article},
	abstract = {1-Methyl- and 1-ethyl-5,6-diphenylpyrazin-2-one crystallize in two modifications, one of which is light-stable and the other light-sensitive. The light-sensitive modification is known to undergo photodimerization in the solid state. This polymorph crystallizes in the monoclinic space group P2(1) with two crystallographically independent molecules in the asymmetric unit. The molecules are packed in stacks running parallel to the unique b axis. The two independent molecules are arranged alternately along the stack. In principle, there are two different pairs of molecules within a stack that can undergo photodimerization, and each should form a different enantiomer. A large crystal was irradiated and a solution of the product was separated by HPLC. The optical purity of the (+)-enantiomer sample was estimated to be greater than 90 \%. This finding indicates that only one of the two pairs undergoes photoreaction. The structure of a single crystal of the pyrazinone was elucidated by X-ray diffractometry before and after irradiation with a laser at a wavelength of 488 nm to 19 \% conversion. The results of the crystal-structure determinations provide additional evidence that only one of the two pairs of molecules undergoes photodimerization although there are no significant differences between the distances between the reacting centers. Furthermore, the latter results suggest that weak hydrogen bonds are a dominant factor that determines which of the two pairs is dimerized upon irradiation. ((C) Wiley-VCH Verlag GmbH \& Co. KGaA, 69451 Weinheim, Germany, 2005).},
	keywords = {chirality, crystal structure, DIMERIZATION, enantioselectivity, PHOTOCHEMISTRY, SINGLE-CRYSTAL PHOTODIMERIZATION, solid-state reactions},
	isbn = {1434-193X},
	url = {<Go to ISI>://000227426900009},
	author = {Kaftory, M. and Shteiman, V. and Lavy, T. and Scheffer, J. R. and Yang, M. and Enkelmann, V.}
}
@article {1229,
	title = {Hydroxytrimethylarsonium iodide, [Me3AsOH]I},
	journal = {Applied Organometallic Chemistry},
	volume = {19},
	number = {3},
	year = {2005},
	note = {ISI Document Delivery No.: 912OSTimes Cited: 0Cited Reference Count: 7},
	month = {Mar},
	pages = {384-385},
	type = {Article},
	abstract = {Hydroxytrimethylarsonium iodide, [Me3AsOH]I, was obtained from the reaction of Me2AsI and MeI in strong basic aqueous solution. The arsenic atom, lying on a mirror plane, is surrounded by one OH and three Me groups, forming a tetrahedral centre. Copyright (c) 2005 John Wiley \& Sons, Ltd.},
	keywords = {arsenic, crystal structure, Mayer reaction, OXIDE, TRIMETHYLARSINE, trimethylhydroxyarsonium iodide},
	isbn = {0268-2605},
	url = {<Go to ISI>://000228089400018},
	author = {Patrick, B. O. and Sun, H. S. and Fricke, M. W. and Cullen, W. R.}
}
@article {643,
	title = {From the first to the second domain of gelsolin: a common path on the surface of actin?},
	journal = {Febs Letters},
	volume = {552},
	number = {2-3},
	year = {2003},
	note = {ISI Document Delivery No.: 726DKTimes Cited: 22Cited Reference Count: 29},
	month = {Sep},
	pages = {86-90},
	type = {Article},
	abstract = {We present the 2.6. resolution crystal structure of a complex formed between G-actin and gelsolin fragment Met25-GIn160 (G1+). The structure differs from those of other gelsolin domain 1 (G1) complexes in that an additional six amino acid residues from the crucial linker region into gelsolin domain 2 (G2) are visible and are attached securely to the surface of actin. The linker segment extends away from G1 up the face of actin in a direction that infers G2 will bind along the same long-pitch helical strand as the actin bound to G1. This is consistent with a mechanism whereby G2 attaches gelsolin to the side of a filament and then directs G1 toward a position where it would disrupt actin-actin contacts. Alignment of the sequence of the structurally important residues within the G1-G2 linker with those of WH2 (WASp homology domain 2) domain protein family members (e.g. WASp (Wiscott-Aldridge syndrome protein) and thymosin beta4) suggests that the opposing activities of filament assembly and disassembly may exploit a common patch on the surface of actin. (C) 2003 Published by Elsevier B.V. on behalf of the Federation of European Biochemical Societies.},
	keywords = {actin, BINDING, calcium, COMPLEX, crystal structure, DIFFRACTION DATA, F-ACTIN, FILAMENT, gelsolin, IDENTIFICATION, MODEL, MOTILITY, NUCLEATION, WH2 domain},
	isbn = {0014-5793},
	url = {<Go to ISI>://000185583000003},
	author = {Irobi, E. and Burtnick, L. D. and Urosev, D. and Narayan, K. and Robinson, R. C.}
}
@article {651,
	title = {Oxidative addition of halogens to MoRu(CO)(6)(dppm)(2)},
	journal = {Inorganic Chemistry Communications},
	volume = {6},
	number = {9},
	year = {2003},
	note = {ISI Document Delivery No.: 720EATimes Cited: 2Cited Reference Count: 27},
	month = {Sep},
	pages = {1175-1179},
	type = {Article},
	abstract = {Halogens oxidatively add to MoRu(CO)(6)(mu-dppm)(2) (1) at ambient temperature to yield [(CO)(2)Mo(mu-X)(mu-CO)(mu-dpmm)(2)Ru(CO)(2)] (divided by)[Mo(CO)(4) X-3](-), where X = Cl (2) or I (3), dppm - Ph2PCH2PPh2, and the mu-CO is semi-bridging. Complexes 2 and 3 have been characterized by elemental analysis, conductivity, and NMR spectroscopy, while the molecular structure of 3 has been determined by X-ray crystallography. Ignoring a weak metal-metal bond interaction, the cation of 3 is most easily described as pseudo-octahedral at Ru(II) and Mo(0) centres; the anion is a monocapped octahedron that has been described previously. (C) 2003 Elsevier B.V. All rights reserved.},
	keywords = {COMPLEX RHRE(CO)4(PH2PCH2PPH2)2, crystal structure, CRYSTAL-STRUCTURE, H2S, halogen reactivity, METAL-CARBONYLS, MO, molybdenum complex, MOLYBDENUM(II), RH, RU, ruthenium complex, semi-bridged carbonyl, SULFUR-DIOXIDE, {bis(diphenylphosphino)methane},
	isbn = {1387-7003},
	url = {<Go to ISI>://000185247500003},
	author = {Khorasani-Motlagh, M. and Safari, N. and Pamplin, C. B. and Patrick, B. O. and James, Brian R.}
}
@article {4851,
	title = {Diphenylboron complexes of the enol tautomers of arylpyruvic acids. Crystal and molecular structure of triethylammonium (2-nitrophenyl)pyruvato-diphenylboron(1-)},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {78},
	number = {5},
	year = {2000},
	note = {ISI Document Delivery No.: 318FFTimes Cited: 2Cited Reference Count: 28},
	month = {Aug},
	pages = {546-552},
	type = {Article},
	abstract = {{Synthesis has been carried out of 15 examples of anionic diphenylboron complexes of arylpyruvic acids, and the structures of the compounds have been determined from spectroscopic data and from X-ray analysis of one of the compounds. Crystals of 5j are monoclinic, P2(1)/n},
	keywords = {arylpyruvic acids, boron complexes, Chelates, crystal structure, diphenylboron, enol tautomers, organoborate salts, PHENYLPYRUVIC ACID},
	isbn = {0008-4042},
	url = {<Go to ISI>://000087272700005},
	author = {Kliegel, W. and Pokriefke, J. O. and Rettig, S. J. and Trotter, J.}
}
@article {4850,
	title = {Structural studies of organoboron compounds, Part 72 - Nitrones and oximes of bifunctional carbonyl compounds and their reaction products with diarylborinic acids. Crystal and molecular structure of examples of five-, six-, and seven-membered boron chelat},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {78},
	number = {10},
	year = {2000},
	note = {ISI Document Delivery No.: 366QGTimes Cited: 9Cited Reference Count: 74},
	month = {Oct},
	pages = {1325-1344},
	type = {Article},
	abstract = {{Synthesis has been carried out of diarylboron chelates of 2- and 3-hydroxynitrones, of 2- and 3-hydroxyoximes, and of 2-carboxynitrones and a 2-carboxyoxime. The structures have been determined from spectroscopic data and from X-ray analyses of 5d, 9a, 11b, and 19. Crystals (at 180 K) of 5d are monoclinic},
	keywords = {carboxynitrones, carboxyoximes, CHEMISTRY, COBALT(III), crystal structure, DERIVATIVES, diarylboron chelates, DIPHENYLBORINIC ACID, hydroxynitrones, HYDROXYOXIME STRUCTURE, hydroxyoximes, LIGAND, METAL-COMPLEXES, N-(2-HYDROXYALKYL)NITRONES, ORGANOBORON COMPOUNDS, RING-CHAIN ISOMERISM},
	isbn = {0008-4042},
	url = {<Go to ISI>://000090015600009},
	author = {Kliegel, W. and Lubkowitz, G. and Pokriefke, J. O. and Rettig, S. J. and Trotter, J.}
}
@article {4642,
	title = {The methylgallium-2-carboxylatobenzimidazolato hexamer, [MeGa center dot C8H4N2O2](6)center dot C6H6 center dot(Me2C6H4)(2); synthesis and X-ray crystal structure},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {77},
	number = {4},
	year = {1999},
	note = {ISI Document Delivery No.: 204JXTimes Cited: 12Cited Reference Count: 18},
	month = {Apr},
	pages = {434-438},
	type = {Article},
	abstract = {{The room-temperature reaction of Me3Ga with benzimidazole 2-carboxylic acid in xylene solvent has yielded a novel crystalline hexameric gallium compound with "MeGa" moieties bridged by the doubly depronotated ligand precursor. Crystals of [MeGa(4,5-benzimidazolato-2-carboxylato)](6).(C6H6).(m-Me2C6H4)(2) are monoclinic},
	keywords = {3, 5-DIMETHYLPYRAZOLATE, benzene intercalate, benzimidazolecarboxylic acid, COMPLEXES, crystal structure, gallium, METALLOCENES},
	isbn = {0008-4042},
	url = {<Go to ISI>://000080762100004},
	author = {Rettig, S. J. and Storr, A. and Trotter, J.}
}
@article {4642,
	title = {The methylgallium-2-carboxylatobenzimidazolato hexamer, [MeGa center dot C8H4N2O2](6)center dot C6H6 center dot(Me2C6H4)(2); synthesis and X-ray crystal structure},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {77},
	number = {4},
	year = {1999},
	note = {ISI Document Delivery No.: 204JXTimes Cited: 12Cited Reference Count: 18},
	month = {Apr},
	pages = {434-438},
	type = {Article},
	abstract = {{The room-temperature reaction of Me3Ga with benzimidazole 2-carboxylic acid in xylene solvent has yielded a novel crystalline hexameric gallium compound with "MeGa" moieties bridged by the doubly depronotated ligand precursor. Crystals of [MeGa(4,5-benzimidazolato-2-carboxylato)](6).(C6H6).(m-Me2C6H4)(2) are monoclinic},
	keywords = {3, 5-DIMETHYLPYRAZOLATE, benzene intercalate, benzimidazolecarboxylic acid, COMPLEXES, crystal structure, gallium, METALLOCENES},
	isbn = {0008-4042},
	url = {<Go to ISI>://000080762100004},
	author = {Rettig, S. J. and Storr, A. and Trotter, J.}
}
@article {4386,
	title = {Coordination complexes derived from 3,6-di(2-pyridyl)-1,4-dihydro-1,2,4,5-tetrazine (DPDHT). Synthesis and molecular structure of [(DPT)(GaMe2)2]},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {76},
	number = {12},
	year = {1998},
	note = {ISI Document Delivery No.: 180RKTimes Cited: 3Cited Reference Count: 25},
	month = {Dec},
	pages = {1800-1804},
	type = {Article},
	abstract = {{The facile reaction of 3,6-di(2-pyridyl)-1,4-dihydro-1,2,4,5-tetrazine (DPDHT) (1) with trimethylgallium has resulted in the formation of the purple crystalline product, [(DPT)(GaMe2)(2)] (2), via methane elimination. Crystals of [(DPT)(GaMe2)(2)] are orthorhombic, Pbca},
	keywords = {3, 5-DIMETHYLPYRAZOLATE, crystal structure, dipyridyldihydrotetrazine, MAGNETIC-PROPERTIES, METAL PYRAZOLATE POLYMERS, METALLOCENES, methylgallium},
	isbn = {0008-4042},
	url = {<Go to ISI>://000079398800003},
	author = {Preston, P. N. and Rettig, S. J. and Storr, A. and Trotter, J.}
}
@article {4386,
	title = {Coordination complexes derived from 3,6-di(2-pyridyl)-1,4-dihydro-1,2,4,5-tetrazine (DPDHT). Synthesis and molecular structure of [(DPT)(GaMe2)2]},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {76},
	number = {12},
	year = {1998},
	note = {ISI Document Delivery No.: 180RKTimes Cited: 3Cited Reference Count: 25},
	month = {Dec},
	pages = {1800-1804},
	type = {Article},
	abstract = {{The facile reaction of 3,6-di(2-pyridyl)-1,4-dihydro-1,2,4,5-tetrazine (DPDHT) (1) with trimethylgallium has resulted in the formation of the purple crystalline product, [(DPT)(GaMe2)(2)] (2), via methane elimination. Crystals of [(DPT)(GaMe2)(2)] are orthorhombic, Pbca},
	keywords = {3, 5-DIMETHYLPYRAZOLATE, crystal structure, dipyridyldihydrotetrazine, MAGNETIC-PROPERTIES, METAL PYRAZOLATE POLYMERS, METALLOCENES, methylgallium},
	isbn = {0008-4042},
	url = {<Go to ISI>://000079398800003},
	author = {Preston, P. N. and Rettig, S. J. and Storr, A. and Trotter, J.}
}
@article {4310,
	title = {Structural studies of organoboron compounds LXIX - Reaction of ketoximes with aliphatic aldehydes and diphenylborinic acid. Crystal and molecular structure of a diphenylboron chelate derived from the pivaldehyde adduct to cyclohexanone oxime},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {76},
	number = {12},
	year = {1998},
	note = {ISI Document Delivery No.: 180RKTimes Cited: 1Cited Reference Count: 15},
	month = {Dec},
	pages = {1789-1795},
	type = {Article},
	abstract = {{Various ketoximes have been reacted with aliphatic aldehydes in the presence of oxybis(diphenylborane) in order to assess the influence of increasingly bulky residues on the nature of the products. Crystals of 5-tert-butyl-2-cyclohexylidene-3,3 -diphenyl-1,4-dioxa-2-azonia-3-boratacyclopentane, 4c, are monoclinic},
	keywords = {crystal structure, ketoximes, ORGANOBORON COMPOUNDS},
	isbn = {0008-4042},
	url = {<Go to ISI>://000079398800001},
	author = {Kliegel, W. and Riebe, U. and Rettig, S. J. and Trotter, J.}
}
@article {4024,
	title = {Novel boron chelate complexes from the reaction of salicylaldehydes, tertiary amines, and diphenylborinic or phenylboronic acid. Crystal and molecular structures of two new types of chelated organoborate salts},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {75},
	number = {9},
	year = {1997},
	note = {ISI Document Delivery No.: YE063Times Cited: 5Cited Reference Count: 29},
	month = {Sep},
	pages = {1203-1214},
	type = {Article},
	abstract = {{The one-pot reaction of equimolar amounts of salicylaldehyde, diphenylborinic acid anhydride, and a tertiary amine in the presence of an alkanol (R{\textquoteright}OH) led to the addition of R{\textquoteright}OH to the aldehyde group and the formation of an O,O-acetal moiety within the chelate anion with the charge balanced by an ammonium cation arising from the tertiary amine. Exchanging the diphenylborinic acid in the three-component reaction system for phenylboronic acid did not give the analogous adduct or chelate but one additional mole equivalent of phenylboronic acid (anhydride) was incorporated, leading to a polycyclic anion containing pyroboronate and acetal boronate functions with an associated ammonium cation. Crystals of 1-methylpiperidinium 4-ethoxy-2,2-dipheny1-1,3-dioxa-2-borata-1,2,3,4-tetrahydronaphthalenate , 6d, are monoclinic},
	keywords = {bisboronate, crystal structure, organoboron compound, SALICYLALDEHYDE, salicylaldehyde semiacetal diphenylboron chelate},
	isbn = {0008-4042},
	url = {<Go to ISI>://A1997YE06300007},
	author = {Kliegel, W. and Metge, J. and Rettig, S. J. and Trotter, J.}
}
@article {4090,
	title = {Synthesis of perfluorodiphenylphosphinic acid and its potassium and oxonium salts; Crystal structure of oxonium perfluorodiphenylphosphinate},
	journal = {Journal of Fluorine Chemistry},
	volume = {83},
	number = {1},
	year = {1997},
	note = {ISI Document Delivery No.: XJ678Times Cited: 9Cited Reference Count: 14},
	month = {Jun},
	pages = {47-50},
	type = {Article},
	abstract = {{The syntheses of perfluorodiphenylphosphinic acid, oxonium perfluorodiphenylphosphinate (perfluorodiphenylphosphinic acid monohydrate), and the potassium salt are described. Crystals of(C6F5)(2)PO2-H2O+ [(C6F5)(2)PO(OH). H2O] are monoclinic},
	keywords = {crystal structure, oxonium perfluorodiphenylphosphinate, perfluorodiphenylphosphinic acid, SYNTHESIS},
	isbn = {0022-1139},
	url = {<Go to ISI>://A1997XJ67800008},
	author = {Oliver, K. W. and Rettig, S. J. and Thompson, R. C. and Trotter, J. and Xia, S. H.}
}
@article {4090,
	title = {Synthesis of perfluorodiphenylphosphinic acid and its potassium and oxonium salts; Crystal structure of oxonium perfluorodiphenylphosphinate},
	journal = {Journal of Fluorine Chemistry},
	volume = {83},
	number = {1},
	year = {1997},
	note = {ISI Document Delivery No.: XJ678Times Cited: 9Cited Reference Count: 14},
	month = {Jun},
	pages = {47-50},
	type = {Article},
	abstract = {{The syntheses of perfluorodiphenylphosphinic acid, oxonium perfluorodiphenylphosphinate (perfluorodiphenylphosphinic acid monohydrate), and the potassium salt are described. Crystals of(C6F5)(2)PO2-H2O+ [(C6F5)(2)PO(OH). H2O] are monoclinic},
	keywords = {crystal structure, oxonium perfluorodiphenylphosphinate, perfluorodiphenylphosphinic acid, SYNTHESIS},
	isbn = {0022-1139},
	url = {<Go to ISI>://A1997XJ67800008},
	author = {Oliver, K. W. and Rettig, S. J. and Thompson, R. C. and Trotter, J. and Xia, S. H.}
}
@article {3718,
	title = {Structural studies of organoboron compounds .64. Boron chelate formation with glycolohydroxamic acids, and the crystal and molecular structure of 5-(1-hydroxycyclohexyl)-2,2-diphenyl-1,3-dioxa-4-azonia-2-borata-4-cyclo pentane},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {74},
	number = {3},
	year = {1996},
	note = {ISI Document Delivery No.: UF848Times Cited: 4Cited Reference Count: 26},
	month = {Mar},
	pages = {445-452},
	type = {Article},
	abstract = {{The syntheses of representative diphenyl- and difluoroboron chelates of 2-hydroxycarbohydroxamic acids (glycolohydroxamic acids) are reported. Crystals of 5-(1-hydroxycyclohexyl)-2,2-diphenyl-1,3-dioxa-4-azonia-2-borata-4-cyclo pentene, 2a, are triclinic},
	keywords = {BOND LENGTHS RELATIONS, crystal structure, HETERO-PI-SYSTEMS, hydroxamatoborate, HYDROXAMIC ACIDS, organoboron compound},
	isbn = {0008-4042},
	url = {<Go to ISI>://A1996UF84800018},
	author = {Kliegel, W. and Schumacher, U. and Rettig, S. J. and Trotter, J.}
}
@article {3806,
	title = {Synthesis, characterization, and reactivity of a ruthenium(II) N,N{\textquoteright},N{\textquoteright}{\textquoteright}-tris(2-pyridyl)phosphine complex. X-ray analysis of RuCl2(PPh(3))(Ppy(3)) (py equals 2-pyridyl)},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {74},
	number = {11},
	year = {1996},
	note = {ISI Document Delivery No.: WC124Times Cited: 10Cited Reference Count: 32},
	month = {Nov},
	pages = {2064-2072},
	type = {Article},
	abstract = {{Reaction of RuCl2(PPh(3))(3) with Ppy(3) (py = 2-pyridyl) in benzene produced the N,N{\textquoteright},N {\textquoteright}{\textquoteright}-Ppy(3) complex RuCl2(PPh(3))(Ppy(3)) 1. Crystals of RuCl2(PPh(3))(Ppy(3)). 2CH(2)Cl(2)(C35H31Cl6N3P2Ru) are monoclinic},
	keywords = {COORDINATION, crystal structure, CRYSTAL-STRUCTURE, LIGANDS, MOLECULAR-STRUCTURES, phosphine, pyridylphosphines, ruthenium},
	isbn = {0008-4042},
	url = {<Go to ISI>://A1996WC12400022},
	author = {Schutte, R. P. and Rettig, S. J. and James, Brian R.}
}
@article {3264,
	title = {THE ONE-STEP SYNTHESIS OF CHIRAL AMINO PHOSPHINO FERROCENES},
	journal = {Journal of Organometallic Chemistry},
	volume = {492},
	number = {2},
	year = {1995},
	note = {ISI Document Delivery No.: QV350Times Cited: 10Cited Reference Count: 24},
	month = {May},
	pages = {157-164},
	type = {Article},
	abstract = {Reaction of the chiral lithium reagent-2-lithio-(alpha-N,N-dimethyl)aminoethylbenzene with 1,1{\textquoteright}-ferrocenediylphenylphosphine gives chiral aminophosphinoferrocenes that contain both chiral carbon and phosphorus centres. Treatment of the ferroceno-phane with 2-lithio-N,N-dimethylaminomethylferrocene followed by hydrolysis gives the product ferrocenyl 2-(dimethylaminomethylferrocenyl) phenylphosphine as a pair of diastereomers. The single crystal structures of compound 3a PdCl2 and compound 4. PdCl2.2CH(2)Cl(2) have been determined. The compounds, 2-(ferrocenylphenylphosphino)-1-(alpha-N, N{\textquoteright}-dimethylaminoethylbenzene)ferrocene, 5 and 1-[2-(alpha-N,N{\textquoteright}-dimethyraminoethylbenzene)phenylphospphino]-1{\textquoteright}-diphenyl phosphinoferrocene, 6a, have also been prepared by minor modifications of the methodology developed.},
	keywords = {<1>FERROCENOPHANES, ASYMMETRIC-SYNTHESIS, CATALYST, chirality, crystal structure, FERROCENE, GRIGNARD, HALIDES, HYDROGENATION, iron, METAL-COMPLEXES, ORGANIC, palladium, PHOSPHORUS, PLANAR CHIRALITY, REAGENTS, SECONDARY},
	isbn = {0022-328X},
	url = {<Go to ISI>://A1995QV35000005},
	author = {Butler, I. R. and Cullen, W. R. and Rettig, S. J. and White, A. S. C.}
}
@article {3452,
	title = {STRUCTURAL STUDIES ON DIMETHYLTIN(IV) CARBOXYLATES},
	journal = {Zeitschrift Fur Anorganische Und Allgemeine Chemie},
	volume = {621},
	number = {11},
	year = {1995},
	note = {ISI Document Delivery No.: TC950Times Cited: 6Cited Reference Count: 23},
	month = {Nov},
	pages = {1875-1882},
	type = {Article},
	abstract = {{In order to correlate Sn-119 Mossbauer parameters and structural data for dimethyltin(IV) derivatives, the molecular structures of bis(acetato)dimethyltin(IV) and bis(trifluoroace tato)dimethyltin(IV) were determined by single crystal X-ray diffration. Crystals of Me(2)Sn(OOCCH3)(2) are monoclinic},
	keywords = {ACIDS, BIS(ACETATO)DIMETHYLTIN(IV), BIS(TRIFLUOROACETATO)DIMETHYLTIN(IV), C-13 NMR, crystal structure, ME2SN(OAC)2, SALTS, X-RAY},
	isbn = {0044-2313},
	url = {<Go to ISI>://A1995TC95000008},
	author = {Mistry, F. and Rettig, S. J. and Trotter, J. and Aubke, F.}
}
@article {3452,
	title = {STRUCTURAL STUDIES ON DIMETHYLTIN(IV) CARBOXYLATES},
	journal = {Zeitschrift Fur Anorganische Und Allgemeine Chemie},
	volume = {621},
	number = {11},
	year = {1995},
	note = {ISI Document Delivery No.: TC950Times Cited: 6Cited Reference Count: 23},
	month = {Nov},
	pages = {1875-1882},
	type = {Article},
	abstract = {{In order to correlate Sn-119 Mossbauer parameters and structural data for dimethyltin(IV) derivatives, the molecular structures of bis(acetato)dimethyltin(IV) and bis(trifluoroace tato)dimethyltin(IV) were determined by single crystal X-ray diffration. Crystals of Me(2)Sn(OOCCH3)(2) are monoclinic},
	keywords = {ACIDS, BIS(ACETATO)DIMETHYLTIN(IV), BIS(TRIFLUOROACETATO)DIMETHYLTIN(IV), C-13 NMR, crystal structure, ME2SN(OAC)2, SALTS, X-RAY},
	isbn = {0044-2313},
	url = {<Go to ISI>://A1995TC95000008},
	author = {Mistry, F. and Rettig, S. J. and Trotter, J. and Aubke, F.}
}
@article {7148,
	title = {THE CRYSTAL AND MOLECULAR-STRUCTURE OF GOLD TRIS(FLUOROSULFATE)},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {69},
	number = {3},
	year = {1991},
	note = {ISI Document Delivery No.: FE808Times Cited: 18Cited Reference Count: 49},
	month = {Mar},
	pages = {391-396},
	type = {Article},
	abstract = {{Single crystals of gold(III) tris(fluorosulfate) are obtained by recrystallization from bis(fluorosulfuryl) peroxide, S2O6F2, under O2 pressure. The crystals of [Au(SO3F)3]2 are monoclinic},
	keywords = {CATIONS, CHEMISTRY, COMPLEXES, crystal structure, GOLD(III) FLUOROSULFATE, GOLD(III) TRIS(FLUOROSULFATE), HSO3F, ION, OXIDE, STABILITY},
	isbn = {0008-4042},
	url = {<Go to ISI>://A1991FE80800005},
	author = {Willner, H. and Rettig, S. J. and Trotter, J. and Aubke, F.}
}
@article {7148,
	title = {THE CRYSTAL AND MOLECULAR-STRUCTURE OF GOLD TRIS(FLUOROSULFATE)},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {69},
	number = {3},
	year = {1991},
	note = {ISI Document Delivery No.: FE808Times Cited: 18Cited Reference Count: 49},
	month = {Mar},
	pages = {391-396},
	type = {Article},
	abstract = {{Single crystals of gold(III) tris(fluorosulfate) are obtained by recrystallization from bis(fluorosulfuryl) peroxide, S2O6F2, under O2 pressure. The crystals of [Au(SO3F)3]2 are monoclinic},
	keywords = {CATIONS, CHEMISTRY, COMPLEXES, crystal structure, GOLD(III) FLUOROSULFATE, GOLD(III) TRIS(FLUOROSULFATE), HSO3F, ION, OXIDE, STABILITY},
	isbn = {0008-4042},
	url = {<Go to ISI>://A1991FE80800005},
	author = {Willner, H. and Rettig, S. J. and Trotter, J. and Aubke, F.}
}
@article {7049,
	title = {STRUCTURAL STUDIES OF ORGANOBORON COMPOUNDS .42. 4,6-BIS(1-CYANO-1-METHYLETHYL)-2-MESITYL-1,3-DIOXA-4,6-DIAZA-2-BORACYCLO HEXANE},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {69},
	number = {2},
	year = {1991},
	note = {ISI Document Delivery No.: FA876Times Cited: 9Cited Reference Count: 28},
	month = {Feb},
	pages = {234-238},
	type = {Article},
	abstract = {{The condensation of N,N{\textquoteright}-bis(1-cyano-1-methylethyl)-N,N{\textquoteright}-dihydroxymethanediamine and mesitylboronic acid gives 4,6-bis(1-cyano-1-methylethyl)-2-mesityl-1,3-dioxa-4,6-diaza-2-boracyclo hexane in good yield. Crystals of the latter compound are orthorhombic},
	keywords = {BORON COMPOUND, CONFORMATION, CRYSTAL, crystal structure, organoboron compound},
	isbn = {0008-4042},
	url = {<Go to ISI>://A1991FA87600010},
	author = {Kliegel, W. and Lubkowitz, G. and Rettig, S. J. and Trotter, J.}
}
@article {7053,
	title = {STRUCTURAL STUDIES OF ORGANOBORON COMPOUNDS .43. 4-[(1-HYDROXYCYCLOHEXYL)METHYL]-2,2,5-TRIPHENYL-1,3-DIOXA-4-AZONIA-2-BOR ATA-4-CYCLOPENTENE},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {69},
	number = {3},
	year = {1991},
	note = {ISI Document Delivery No.: FE808Times Cited: 7Cited Reference Count: 23},
	month = {Mar},
	pages = {545-549},
	type = {Article},
	abstract = {{The reaction of N{\textquoteright}-hydroxy-N-[1-hydroxycyclohexyl)methyl]benzamide and diphenylborinic anhydride gives 4-[(1-hydroxycyclohexyl)methyl]-2,2,5-triphenyl-1,3-dioxa-4-azonia-2-bor ata-4-cyclopentene in nearly quantitative yield. Crystals of the product are monoclinic},
	keywords = {BOND LENGTHS RELATIONS, BORON COMPOUND, CN-BONDS, CO-BONDS, CRYSTAL, crystal structure, HETERO-PI-SYSTEMS, MOLECULAR-STRUCTURES, organoboron compound},
	isbn = {0008-4042},
	url = {<Go to ISI>://A1991FE80800027},
	author = {Kliegel, W. and Schumacher, U. and Tajerbashi, M. and Rettig, S. J. and Trotter, J.}
}
@article {7054,
	title = {STRUCTURAL STUDIES OF ORGANOBORON COMPOUNDS .44. 2,3-DIHYDRO-3-HYDROXY-2,2-TETRAMETHYLENE-4H-BENZOXAZIN-4-ONE AND ITS DIFLUOROBORON CHELATE, 2,2-DIFLUORO-4,4-TETRAMETHYLENE-1,3,5-TRIOXA-3A-AZONIA-2-BORATA-2,3,4,5- TETRAHYDRO-1H-CYCLOPENTA[A]NAPHTHALENE},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {69},
	number = {4},
	year = {1991},
	note = {ISI Document Delivery No.: FL979Times Cited: 4Cited Reference Count: 28},
	month = {Apr},
	pages = {673-680},
	type = {Article},
	abstract = {{The reaction of 2,3-dihydro-3-hydroxy-2,2-tetramethylene-4H-benzoxazin-4-one, 2, and diethyl ether-boron trifluoride yields the difluoroboron chelate 2,2-difluoro-4,4-tetramethylene-1,3,5-trioxa-3a-azonia-2-borata-2,3,4,5- tetrahydro-1H-cyclopenta[a]naphthalene, 6, in high yield. There are two crystal forms of 2: 2a, triclinic, P1BAR},
	keywords = {ADJACENT ACYL LIGANDS, ANALOGS, BORON COMPOUND, CARBON BOND FORMATION, COMPLEXES, COORDINATED MOLECULES, CRYSTAL, crystal structure, organoboron compound, RING},
	isbn = {0008-4042},
	url = {<Go to ISI>://A1991FL97900014},
	author = {Kliegel, W. and Tajerbashi, M. and Rettig, S. J. and Trotter, J.}
}
@article {7052,
	title = {STRUCTURAL STUDIES OF ORGANOBORON COMPOUNDS .45. 5,5-DIFLUORO-2,2-PENTAMETHYLENE-7,7-DIPHENYL-1,4,6-TRIOXA-3A-AZONIA-5-BO RATA-2,3,4,5,6,7-HEXAHYDROINDENE},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {69},
	number = {4},
	year = {1991},
	note = {ISI Document Delivery No.: FL979Times Cited: 5Cited Reference Count: 26},
	month = {Apr},
	pages = {681-686},
	type = {Article},
	abstract = {{The reaction of N,2-dihydroxy-N-(1-hydroxycyclohexyl)methyl-2,2-diphenylacetamide with dimethyl ether-boron trifluoride gives 5,5-difluoro-2,2-pentamethylene-7,7-diphenyl-1,4,6-trioxa-3a-azonia-5-bo rata-2,3,4,5,6,7-hexahydroindene in nearly quantitative yield. Crystals of the product are triclinic},
	keywords = {ACIDS, BOND LENGTHS, BORON COMPOUND, CRYSTAL, crystal structure, MOLECULAR-STRUCTURE, NITRONES, organoboron compound, OXAZOLINE N-OXIDES},
	isbn = {0008-4042},
	url = {<Go to ISI>://A1991FL97900015},
	author = {Kliegel, W. and Schumacher, U. and Rettig, S. J. and Trotter, J.}
}
@article {7051,
	title = {STRUCTURAL STUDIES OF ORGANOBORON COMPOUNDS .46. 5,5-PENTAMETHYLENE-2-PHENYL-4,5-DIHYDROOXAZOL-N-OXIDE(N-O-B)TRIFLUOROBOR ANE},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {69},
	number = {8},
	year = {1991},
	note = {ISI Document Delivery No.: GC235Times Cited: 4Cited Reference Count: 26},
	month = {Aug},
	pages = {1212-1216},
	type = {Article},
	abstract = {{The reaction of N-hydroxy-N-[(1-hydroxycyclohexyl)methyl]benzamide with dimethylether-boron trifluoride gives 5,5-penta-methylene-2-phenyl-4,5-dihydrooxazol-N-oxide(N-O-B)trifluorobo rane [3-(2,2,2-trifluoro-1-oxa-2-borataethyl)-5,5-pentamethylene-2-phenyl-1-o xa-3-azonia-2-cyclopentene] in high yield. Crystals of the product are monoclinic},
	keywords = {BORON, BORON COMPOUND, CRYSTAL, crystal structure, MOLECULAR-STRUCTURE, organoboron compound},
	isbn = {0008-4042},
	url = {<Go to ISI>://A1991GC23500006},
	author = {Kliegel, W. and Schumacher, U. and Rettig, S. J. and Trotter, J.}
}
@article {7047,
	title = {STRUCTURAL STUDIES OF ORGANOBORON COMPOUNDS .47. 6,8-BIS(1-CYANO-1-METHYLETHYL)-2,4-DIPHENYL-1,3,5-TRIOXA-6,8-DIAZA-2,4-D IBORACYCLOOCTANE},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {69},
	number = {8},
	year = {1991},
	note = {ISI Document Delivery No.: GC235Times Cited: 7Cited Reference Count: 16},
	month = {Aug},
	pages = {1217-1221},
	type = {Article},
	abstract = {{The reaction of N,N{\textquoteright}-bis (1-cyano-1-methylethyl)-N,N{\textquoteright}-dihydroxymethanediamine with phenylbnronic acid gives 6,8-bis(-1-cyano-1-methylethy)-2,4-diphenyl-1,3,5-trioxa-6,8-diaza-2,4-d iboracyclooctane in good yield. Crystals of the product are monoclinic},
	keywords = {BORON COMPOUND, CRYSTAL, crystal structure, INCIPIENT NUCLEOPHILIC ADDITIONS, MOLECULAR-STRUCTURE, organoboron compound},
	isbn = {0008-4042},
	url = {<Go to ISI>://A1991GC23500007},
	author = {Kliegel, W. and Lubkowitz, G. and Rettig, S. J. and Trotter, J.}
}
@article {7050,
	title = {STRUCTURAL STUDIES OF ORGANOBORON COMPOUNDS .48. 1,4-DIPHENYL-3,3-6,6-BIS(TETRAMETHYLENE)-2,5,7-TRIOXA-3,6-DIAZONIA-1,4-D IBORATABICYCLO(2.2.1)HEPTANE},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {69},
	number = {8},
	year = {1991},
	note = {ISI Document Delivery No.: GC235Times Cited: 7Cited Reference Count: 33},
	month = {Aug},
	pages = {1222-1226},
	type = {Article},
	abstract = {{The reaction of N-hydroxypyrrolidine with either oxybis(diphenylborane) or phenylboronic acid gives 1,4-diphenyl-3,3:6,6-bis(tetramethylene)-2,5,7-trioxa-3,6-diazoniia-1,4- diboratabicyclo[2.2.1]heptane in moderate yield. Crystals of the product are orthorhombic},
	keywords = {2, 4-DIBORATABICYCLO(2.2.1)HEPTANE RING, 5, 6-DIAZONIA-1, 7-TRIOXA-3, crystal structure, CRYSTAL-STRUCTURE, MOLECULAR-STRUCTURE, organoboron compound, SYSTEM, X-RAY-DIFFRACTION},
	isbn = {0008-4042},
	url = {<Go to ISI>://A1991GC23500008},
	author = {Kliegel, W. and Riebe, U. and Rettig, S. J. and Trotter, J.}
}
@article {7048,
	title = {STRUCTURAL STUDIES OF ORGANOBORON COMPOUNDS .49. 4,6-BIS(1-PHENYL-2-NITROETHYL)-2-(4-METHOXYPHENYL)-1,3-DIOXA-4,6-DIAZA-2 -BORACYCLOHEXANE},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {69},
	number = {8},
	year = {1991},
	note = {ISI Document Delivery No.: GC235Times Cited: 4Cited Reference Count: 23},
	month = {Aug},
	pages = {1227-1232},
	type = {Article},
	abstract = {{The preparation of N,N{\textquoteright}-bis(1-phenyl-2-nitroethyl)-N,N{\textquoteright}-dihydroxymethanediamine and its subsequent reaction with 4-methoxyphenylboronic acid to yield 4,6-bis(1-phenyl-2-nitroethyl)-2-(4-methoxyphenyl)-1,3-dioxa-4,6-diaza-2 -boracyclohexane are described. Crystals of the latter compound are monoclinic},
	keywords = {crystal structure, CYCLOBORONATE, METHANEDIAMINE, NITROGEN, organoboron compound},
	isbn = {0008-4042},
	url = {<Go to ISI>://A1991GC23500009},
	author = {Kliegel, W. and Lubkowitz, G. and Rettig, S. J. and Trotter, J.}
}
@article {7006,
	title = {SYNTHESIS, STRUCTURE, AND MAGNETIC-PROPERTIES OF DIPHENYLPHOSPHINATES OF COBALT(II) AND MANGANESE(II) - THE CRYSTAL AND MOLECULAR-STRUCTURES OF THE GAMMA-FORMS OF POLY-BIS(MU-DIPHENYLPHOSPHINATO)COBALT(II) AND MANGANESE(II)},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {69},
	number = {2},
	year = {1991},
	note = {ISI Document Delivery No.: FA876Times Cited: 16Cited Reference Count: 20},
	month = {Feb},
	pages = {277-285},
	type = {Article},
	abstract = {{The synthesis of the beta and gamma forms of M(Ph2PO2)2 where M = Co and Mn are described and the compounds are characterized by infrared spectroscopy, differential scanning calorimetry, X-ray powder diffraction, and low-temperature (2-80 K) magnetic susceptibility studies. Single crystal X-ray diffraction studies are reported on the gamma forms. Crystals of the gamma forms of poly-bis(mu-diphenylphosphinato)cobalt(II) and poly-bis(mu-diphenylphosphinato)manganese(II) are isomorphous, crystallizing with 4 formula units per unit-cell in the monoclinic space group P2(1)/c. Lattice constants are a = 8.080(2), 8.161(1)},
	keywords = {crystal structure, DIPHENYLPHOSPHINATES OF COBALT(II) AND, EXCHANGE, MAGNETIC PROPERTIES, manganese(II)},
	isbn = {0008-4042},
	url = {<Go to ISI>://A1991FA87600016},
	author = {Du, J. L. and Rettig, S. J. and Thompson, R. C. and Trotter, J.}
}
@article {7006,
	title = {SYNTHESIS, STRUCTURE, AND MAGNETIC-PROPERTIES OF DIPHENYLPHOSPHINATES OF COBALT(II) AND MANGANESE(II) - THE CRYSTAL AND MOLECULAR-STRUCTURES OF THE GAMMA-FORMS OF POLY-BIS(MU-DIPHENYLPHOSPHINATO)COBALT(II) AND MANGANESE(II)},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {69},
	number = {2},
	year = {1991},
	note = {ISI Document Delivery No.: FA876Times Cited: 16Cited Reference Count: 20},
	month = {Feb},
	pages = {277-285},
	type = {Article},
	abstract = {{The synthesis of the beta and gamma forms of M(Ph2PO2)2 where M = Co and Mn are described and the compounds are characterized by infrared spectroscopy, differential scanning calorimetry, X-ray powder diffraction, and low-temperature (2-80 K) magnetic susceptibility studies. Single crystal X-ray diffraction studies are reported on the gamma forms. Crystals of the gamma forms of poly-bis(mu-diphenylphosphinato)cobalt(II) and poly-bis(mu-diphenylphosphinato)manganese(II) are isomorphous, crystallizing with 4 formula units per unit-cell in the monoclinic space group P2(1)/c. Lattice constants are a = 8.080(2), 8.161(1)},
	keywords = {crystal structure, DIPHENYLPHOSPHINATES OF COBALT(II) AND, EXCHANGE, MAGNETIC PROPERTIES, manganese(II)},
	isbn = {0008-4042},
	url = {<Go to ISI>://A1991FA87600016},
	author = {Du, J. L. and Rettig, S. J. and Thompson, R. C. and Trotter, J.}
}
