@article {2352,
	title = {An Improved Synthesis of Pyridine-Thiazole Cores of Thiopeptide Antibiotics},
	journal = {Journal of Organic Chemistry},
	volume = {74},
	number = {15},
	year = {2009},
	note = {ISI Document Delivery No.: 476XOTimes Cited: 4Cited Reference Count: 29Aulakh, Virender S. Ciufolini, Marco A.},
	month = {Aug},
	pages = {5750-5753},
	type = {Article},
	abstract = {The oxidation of 2-methylthiazoles to 2-formylthiazoles simplifies the implementation of the Bagley variant of the Bohlmann-Rahtz reaction as a key step in a concise new route to pyridine cores of thiopeptide antibiotics.},
	keywords = {1ST, AMYTHIAMICIN-D, CONSTRUCTION, GE2270-A, KEY BUILDING-BLOCKS, macrocycle, MICROCOCCIN P1, ONE-POT, PROMOTHIOCIN, SYNTHESIS, THIOSTREPTON},
	isbn = {0022-3263},
	url = {<Go to ISI>://000268480300104},
	author = {Aulakh, V. S. and Ciufolini,Marco A.}
}
@article {2289,
	title = {Capturing aqueous [F-18]-fluoride with an arylboronic ester for PET: Synthesis and aqueous stability of a fluorescent [F-18]-labeled aryltrifluoroborate},
	journal = {Journal of Fluorine Chemistry},
	volume = {129},
	number = {5},
	year = {2008},
	note = {ISI Document Delivery No.: 302SWTimes Cited: 5Cited Reference Count: 12Ting, Richard Lo, Justin Adam, Michael J. Ruth, Thomas J. Perrin, David M.},
	month = {May},
	pages = {349-358},
	type = {Article},
	abstract = {The aqueous stability of aryltrifluoroborates is of importance to their use in transition metal mediated coupling reactions as well as their potential use in [F-18]-labeled aryltrifluoroborate PET imaging agents. Nevertheless, few studies have fully characterized the solvolysis of fluoride from an aryltrifluoroborate in water. Using [F-19] NMR, fluorescence and [F-18]-labeling techniques, we disclose the composition of an aryltrifluoroborate of exceptional kinetic stability with respect to solvolytic defluoridation. This work not only highlights the potential of using [F-18]-labeled aryltrifluoroborates for PET tracers, but provides a chemical platform and a general approach for evaluating the stability of other aryltrifluoroborates. (c) 2008 Elsevier B.V. All rights reserved.},
	keywords = {ACIDS, aryltrifluoroborate, CROSS-COUPLING REACTIONS, KINETICS, PET, SYNTHESIS, [F-18]-labeling},
	isbn = {0022-1139},
	url = {<Go to ISI>://000255990600005},
	author = {Ting, R. and Lo, J. and Adam,Michael J. and Ruth, T. J. and Perrin,David M.}
}
@article {2289,
	title = {Capturing aqueous [F-18]-fluoride with an arylboronic ester for PET: Synthesis and aqueous stability of a fluorescent [F-18]-labeled aryltrifluoroborate},
	journal = {Journal of Fluorine Chemistry},
	volume = {129},
	number = {5},
	year = {2008},
	note = {ISI Document Delivery No.: 302SWTimes Cited: 5Cited Reference Count: 12Ting, Richard Lo, Justin Adam, Michael J. Ruth, Thomas J. Perrin, David M.},
	month = {May},
	pages = {349-358},
	type = {Article},
	abstract = {The aqueous stability of aryltrifluoroborates is of importance to their use in transition metal mediated coupling reactions as well as their potential use in [F-18]-labeled aryltrifluoroborate PET imaging agents. Nevertheless, few studies have fully characterized the solvolysis of fluoride from an aryltrifluoroborate in water. Using [F-19] NMR, fluorescence and [F-18]-labeling techniques, we disclose the composition of an aryltrifluoroborate of exceptional kinetic stability with respect to solvolytic defluoridation. This work not only highlights the potential of using [F-18]-labeled aryltrifluoroborates for PET tracers, but provides a chemical platform and a general approach for evaluating the stability of other aryltrifluoroborates. (c) 2008 Elsevier B.V. All rights reserved.},
	keywords = {ACIDS, aryltrifluoroborate, CROSS-COUPLING REACTIONS, KINETICS, PET, SYNTHESIS, [F-18]-labeling},
	isbn = {0022-1139},
	url = {<Go to ISI>://000255990600005},
	author = {Ting, R. and Lo, J. and Adam,Michael J. and Ruth, T. J. and Perrin,David M.}
}
@article {2205,
	title = {Template-assembled synthetic G-quartets (TASQs)},
	journal = {Angewandte Chemie-International Edition},
	volume = {47},
	number = {26},
	year = {2008},
	note = {ISI Document Delivery No.: 317SSTimes Cited: 8Cited Reference Count: 38Nikan, Mehran Sherman, John C.},
	pages = {4900-4902},
	type = {Article},
	keywords = {cation, CAVITANDS, CHEMISTRY, DEOXYGUANOSINE, DERIVATIVES, G-quartets, GUANOSINE, HOST-GUEST COMPLEXATION, NUCLEOSIDES, NUCLEOTIDE, ORGANIC-SOLVENTS, QUADRUPLEX STRUCTURE, supramolecular, supramolecular chemistry, SYNTHESIS, TELOMERIC DNA OLIGONUCLEOTIDES, TEMPLATE},
	isbn = {1433-7851},
	url = {<Go to ISI>://000257040800022},
	author = {Nikan, M. and Sherman, J. C.}
}
@article {749,
	title = {Briarane, erythrane, and aquariane diterpenoids from the Caribbean gorgonian Erythropodium caribaeorum},
	journal = {European Journal of Organic Chemistry},
	number = {18},
	year = {2003},
	note = {ISI Document Delivery No.: 726HFTimes Cited: 5Cited Reference Count: 15},
	month = {Sep},
	pages = {3515-3523},
	type = {Article},
	abstract = {Seven new diterpenoids belonging to the briarane [erythrolides R (5), S (6), T (7), and U (8)], erythrane [erythrolide V (9)], and aquariane [aquariolides B (10) and C (11)] skeletal classes have been isolated from the encrusting gorgonian Erythropodium caribaeorum. The structures of the new compounds were elucidated by spectroscopic analysis and chemical interconversions. A biogenetic proposal that links carbon skeletons found in E. caribaeorum diterpenoids is presented. (C) Wiley-VCH Verlag GmbH Co.},
	keywords = {asymmetric, bioorganic chemistry, ELEUTHEROBIN, ERYTHROLIDES, natural products, structure elucidation, SYNTHESIS, terpenoids},
	isbn = {1434-193X},
	url = {<Go to ISI>://000185592300005},
	author = {Taglialatela-Scafati, O. and Craig, K. S. and Reberioux, D. and Roberge, M. and Andersen, R. J.}
}
@article {609,
	title = {Interaction of rhodium(I) bisphosphine complexes with semicarbazones to give orthometallated rhodium(III) complexes},
	journal = {Russian Chemical Bulletin},
	volume = {52},
	number = {12},
	year = {2003},
	note = {ISI Document Delivery No.: 809IUTimes Cited: 7Cited Reference Count: 57International Memorial Symposium on Modern Trends in Organometallic and Catalytic Chemistry Dedicated to Mark Vol{\textquoteright}pinMAY 18-AUG 23, 2003Moscow, RUSSIA},
	month = {Dec},
	pages = {2707-2714},
	type = {Proceedings Paper},
	abstract = {Interaction of the cis-[Rh(PR3)(2)(Solv)(2)]PF6 complexes (R = Ar or R-3 = Ph2Me, Solv solvent) under Ar with semicarbazones bearing a phenyl group on the imine-C atom gives the rhodium(III)-hydrido-bis(phosphine)-orthometallated semicarbazone species [RhH(PR3)(2){(o-C6H4(R{\textquoteright})C=N-N(H)CONH2}]PF6 (R{\textquoteright} = Me or Et), which are characterized generally by elemental analysis, P-31{H-1} and H-1 NMR spectroscopy, and mass-spectrometry. The PPh3-containing complex with R{\textquoteright} = Me, structurally characterized by X-ray analysis, reveals coordination of the semicarbazone by the ortho-C atom, the imine-N atom, and the amide-carbonyl group. For a semicarbazone containing no Ph group, the rhodium(I) complex [Rh(PR3)(2)(Et(Me)C=N-N(H)CONH2)]PF6, containing the eta(2)-semicarbazone bonded via the imine-N and carbonyl, is formed. Attempts to hydrogenate the C=N moiety in the complexes or to catalytically hydrogenate the semicarbazones were unsuccessful.},
	keywords = {ACTIVATION, ASYMMETRIC HYDROGENATION, BENZALDEHYDE SEMICARBAZONE, C-H, C-H BONDS, CATALYTIC-HYDROGENATION, COMPLEXES, CRYSTAL-STRUCTURE, FINE CHEMICALS, INTRAMOLECULAR ACTIVATION, molecular structure, orthometallation, phosphines, rhodium, SELECTIVE HYDROGENATION, semicarbazones, SYNTHESIS, TRANSITION-METAL-COMPLEXES, UNPRECEDENTED CHEMICAL TRANSFORMATION},
	isbn = {1066-5285},
	url = {<Go to ISI>://000220631200019},
	author = {Ezhova, M. B. and Patrick, B. O. and James, Brian R. and Ford, M. E. and Waller, E. J.}
}
@article {499,
	title = {Effects of diabetes, vanadium, and insulin on glycogen synthase activation in Wistar rats},
	journal = {Molecular and Cellular Biochemistry},
	volume = {231},
	number = {1-2},
	year = {2002},
	note = {ISI Document Delivery No.: 527LATimes Cited: 21Cited Reference Count: 51},
	month = {Feb},
	pages = {23-35},
	type = {Article},
	abstract = {In vivo effects of insulin and vanadium treatment on glycogen synthase (GS), glycogen synthase kinase-3 (GSK-3) and protein phosphatase-1 (PP1) activity were determined in Wistar rats with streptozotocin (STZ)-induced diabetes. The skeletal muscle was freeze-clamped before or following an insulin injection (5 U/kg i.v.). Diabetes, vanadium, and insulin in vivo treatment did not affect muscle GSK-3beta activity as compared to controls. Following insulin stimulation in 4-week STZ-diabetic rats muscle GS fractional activity (GSFA) was increased 3 fold (p < 0.05), while in 7-week diabetic rats it remained unchanged, suggesting development of insulin resistance in longer term diabetes. Muscle PP1 activity was increased in diabetic rats and returned to normal after vanadium treatment, while muscle GSFA remained unchanged. Therefore, it is possible that PP1 is involved in the regulation of some other cellular events of vanadium (other than regulation of glycogen synthesis). The lack of effect of vanadium treatment in stimulating glycogen synthesis in skeletal muscle suggests the involvement of other metabolic pathways in the observed glucoregulatory effect of vanadium.},
	keywords = {BLOOD-GLUCOSE, GLUCOSE-TRANSPORT, glycogen, IN-VITRO, insulin resistance, MELLITUS, MOLECULAR MECHANISM, PHOSPHORYLATION, PROTEIN-KINASE-B, RABBIT SKELETAL-MUSCLE, S6 KINASE, serine/threonine kinases and phosphatases, streptozotocin-induced diabetes, SYNTHESIS, VANADATE},
	isbn = {0300-8177},
	url = {<Go to ISI>://000174186500004},
	author = {Semiz, S. and Orvig, Chris and McNeill, J. H.}
}
@article {405,
	title = {Synthesis and characterization of polymer brushes of poly(N,N-dimethylacrylamide) from polystyrene-latex by aqueous atom transfer radical polymerization},
	journal = {Macromolecules},
	volume = {35},
	number = {11},
	year = {2002},
	note = {ISI Document Delivery No.: 554GUTimes Cited: 64Cited Reference Count: 51},
	month = {May},
	pages = {4247-4257},
	type = {Article},
	abstract = {Negatively charged polystyrene latex was synthesized, and a copolymer shell of 2-(methyl-2{\textquoteright}-chloropropionato)ethyl acrylate (HEA-Cl) and styrene was added, from which poly(N,N-dimethylacrylamide) (PDMA) was polymerized by atom transfer radical polymerization in aqueous suspension at room temperature. Increasing monomer concentration in the presence of CuCl or CuBr and one of three ligands (N,N,N{\textquoteright},N{\textquoteright},N"-pentamethyldiethylenetriamine (PMDETA), 1,1,4,7,10,10-hexamethyltriethylenetetramine (HMTETA), and tris [2-(dimethylamino)ethyl] amine (Me6TREN)) produced grafts whose molecular weight increased to over 600 000 and polydispersities in the range of 1.3-1.8, determined from chains recovered following cleavage by base. Hydrodynamic brush thicknesses were 70-800 nm, and average chain separations, calculated from M-n and the mass of polymer recovered per particle, varied from 4.0 to 1.1 nm. Very high grafting densities were achieved with good molecular weight control, the highest densities yet reported for high molecular weight polymer chains grown from a surface. Control of the polymerization was improved by addition of Cu(II) to enhance deactivation of free radicals, by including a low concentration of exogenous hydrophobic initiator at high monomer concentration and by reducing latex concentration. Increasing the concentration of exogenous initiator reduced graft thickness but eliminated control over the polydispersity. The unusual conditions required for optimization of the reaction and the observation of decreasing chain separation as M-n increased were explained by invoking a model of the particle surface that took into account the finite depth and high copolymer concentration of the region in which chains were initiated and particularly the fixed charges due to the sulfate initiator of shell copolymerization.},
	keywords = {(METH)ACRYLAMIDES, ADSORPTION, AMBIENT-TEMPERATURE, BLOCK-COPOLYMERS, CARBOCATIONIC, FACILE, POLYELECTROLYTE BRUSHES, POLYMERIZATION, SELF-ASSEMBLED MONOLAYERS, SURFACE, SYNTHESIS, TETHERED CHAINS},
	isbn = {0024-9297},
	url = {<Go to ISI>://000175728100006},
	author = {Jayachandran, K. N. and Takacs-Cox, A. and Brooks, D. E.}
}
@article {4395,
	title = {UDP-N-trifluoroacetylglucosamine as an alternative substrate in N-acetylglucosaminyltransferase reactions},
	journal = {Carbohydrate Research},
	volume = {306},
	number = {1-2},
	year = {1998},
	note = {ISI Document Delivery No.: 100VZTimes Cited: 15Cited Reference Count: 28},
	month = {Jan},
	pages = {127-136},
	type = {Article},
	abstract = {The synthesis of UDP-N-trifluoroacetylglucosamine [uridine 5{\textquoteright}-(2-trifluoroacetamido-2-deoxy-alpha-D-glucopyranosyl diphosphate, UDP-GlcNAc-F-3] is reported. The compound is found to serve as a substrate for the {\textquoteright}core-2{\textquoteright} GlcNAc transferase (EC 2.4.1.102) that is involved in the biosynthesis, of O-linked glycoproteins and for the GlcNAcT-V transferase (EC 2.4. 1.155) that is a key biosynthetic enzyme controlling the branching pattern of cell surface complex Asn-linked oligosaccharides. The trisaccharide beta-o-Gal p-(1 {\textendash}> 3)-[beta-D-GlcpNAc-F-3(1 {\textendash}> 6)]alpha-D-GalpNAc-OR [R = (CH2)(8)CO2Me] was prepared from beta-D-Galp-(1 {\textendash}> 3)-alpha-D-GalpNAc-OR using the {\textquoteright}core-2{\textquoteright} GlcNAc transferase. The tetrasaccharide beta-D-GlcpNAc-(1 {\textendash}> 2)-[beta-D-GlcpNAc-F-3-(1 {\textendash}> 6)]-alpha-D-Manp-(1 {\textendash}> 6)-beta-D-Glcp-OR [R = (CH2)(7)CH3] was prepared from beta-D-GlcpNAc-(1 {\textendash}> 2)-alpha-D-Manp-(1 {\textendash}> 6)-beta-D-Glcp-OR [R = (CH2)(7)CH3] using the GlcNAcT-V transferase. Removal of the trifluoroacetyl group was achieved under mild basic conditions to give the corresponding glucosamine containing tetrasaccharide. These examples demonstrate the feasibility of introducing masked forms of glucosamine residues into oligosaccharides using GlcNAc-specific transferases. The requirement for the trifluoroacetamido group as a specific recognition element was evident in the observation that neither UDP-glucosamine nor UDP-glucose served as a donor substrates for the {\textquoteright}core-2{\textquoteright} GlcNAc transferase. (C) 1998 Elsevier Science Ltd. All rights reserved.},
	keywords = {GLYCOPROTEINS, N-acetylglucosaminyltransferase, OLIGOSACCHARIDE, OLIGOSACCHARIDES, ORGANIC-SYNTHESIS, RECOGNITION, SYNTHESIS, UDP-sugar analog},
	isbn = {0008-6215},
	url = {<Go to ISI>://000074837200012},
	author = {Sala, R. F. and MacKinnon, S. L. and Palcic, M. M. and Tanner, M. E.}
}
@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 {3758,
	title = {2,3-Pyrazinedicarboxylates of cobalt(II), nickel(II), and copper(II); Magnetic properties and crystal structures},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {74},
	number = {3},
	year = {1996},
	note = {ISI Document Delivery No.: UF848Times Cited: 30Cited Reference Count: 28},
	month = {Mar},
	pages = {433-444},
	type = {Article},
	abstract = {{Complexes of singly and doubly deprotonated 2,3-pyrazinedicarboxylic acid (pyzdcH(2)) have been prepared and studied. Crystal data: [Ni(pyzdcH)(2)(H2O)(2)], 1, monoclinic, P2(1)/n},
	keywords = {3-pyrazinedicarboxylates, ANTIFERROMAGNETISM, COMPLEXES, metal 2, SUPEREXCHANGE MECHANISM, SYNTHESIS, X-ray structure},
	isbn = {0008-4042},
	url = {<Go to ISI>://A1996UF84800017},
	author = {Mao, L. and Rettig, S. J. and Thompson, R. C. and Trotter, J. and Xia, S. H.}
}
@article {3758,
	title = {2,3-Pyrazinedicarboxylates of cobalt(II), nickel(II), and copper(II); Magnetic properties and crystal structures},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {74},
	number = {3},
	year = {1996},
	note = {ISI Document Delivery No.: UF848Times Cited: 30Cited Reference Count: 28},
	month = {Mar},
	pages = {433-444},
	type = {Article},
	abstract = {{Complexes of singly and doubly deprotonated 2,3-pyrazinedicarboxylic acid (pyzdcH(2)) have been prepared and studied. Crystal data: [Ni(pyzdcH)(2)(H2O)(2)], 1, monoclinic, P2(1)/n},
	keywords = {3-pyrazinedicarboxylates, ANTIFERROMAGNETISM, COMPLEXES, metal 2, SUPEREXCHANGE MECHANISM, SYNTHESIS, X-ray structure},
	isbn = {0008-4042},
	url = {<Go to ISI>://A1996UF84800017},
	author = {Mao, L. and Rettig, S. J. and Thompson, R. C. and Trotter, J. and Xia, S. H.}
}
@article {3534,
	title = {COORDINATION POLYMERS INCORPORATING WEAKLY COORDINATING FLUOROANIONS},
	journal = {Journal of Fluorine Chemistry},
	volume = {71},
	number = {2},
	year = {1995},
	note = {ISI Document Delivery No.: QV343Times Cited: 1Cited Reference Count: 9George H Cady Symposium on Inorganic Chemistry, at the 207th Meeting of the American-Chemical-SocietyMAR 14-17, 1994SAN DIEGO, CAAMER CHEM SOC},
	month = {Apr},
	pages = {191-191},
	type = {Proceedings Paper},
	keywords = {ANTIFERROMAGNETIC EXCHANGE, coordination polymers, FLUOROANIONS, MAGNETIC EXCHANGE, SINGLE-CRYSTAL X-RAY DIFFRACTION, SYNTHESIS},
	isbn = {0022-1139},
	url = {<Go to ISI>://A1995QV34300020},
	author = {Thompson, R. C.}
}
@article {3255,
	title = {THE USE OF FLUOROSULFURIC ACID, MAGIC ACID AND LIQUID ANTIMONY(V) FLUORIDE AS MEDIA TO GENERATE, STABILIZE AND STUDY METAL-CARBONYL CATIONS},
	journal = {Journal of Fluorine Chemistry},
	volume = {71},
	number = {2},
	year = {1995},
	note = {ISI Document Delivery No.: QV343Times Cited: 0Cited Reference Count: 11George H Cady Symposium on Inorganic Chemistry, at the 207th Meeting of the American-Chemical-SocietyMAR 14-17, 1994SAN DIEGO, CAAMER CHEM SOC},
	month = {Apr},
	pages = {201-202},
	type = {Proceedings Paper},
	keywords = {antimony(V) fluoride, CATIONS, fluorosulfuric acid, IR spectroscopy, magic acid, METAL CARBONYL, NMR spectroscopy, SYNTHESIS, UNDECAFLUORODIANTIMONATE(V)},
	isbn = {0022-1139},
	url = {<Go to ISI>://A1995QV34300025},
	author = {Bodenbinder, M. and Willner, H. and Aubke, F.}
}
@article {6960,
	title = {SYNTHESIS OF ISOCYANO AND (HALOALKYNYL) BIPHENYLS - NEW THERMOTROPIC LIQUID-CRYSTALS},
	journal = {Molecular Crystals and Liquid Crystals},
	volume = {198},
	year = {1991},
	note = {ISI Document Delivery No.: FN646Times Cited: 6Cited Reference Count: 913TH INTERNATIONAL LIQUID CRYSTAL CONFJUL 22-27, 1990VANCOUVER, CANADA},
	pages = {417-428},
	type = {Proceedings Paper},
	keywords = {BIPHENYL, HALOALKYNES, ISOCYANIDES, SYNTHESIS, THERMOTROPICS},
	isbn = {1542-1406},
	url = {<Go to ISI>://A1991FN64600041},
	author = {Bailey, A. L. and Bates, G. S.}
}
