@article {5180,
	title = {Fixation of amine copper preservatives Part 1. Reaction of vanillin, a lignin model compound with monoethanolamine copper sulphate solution},
	journal = {Holzforschung},
	volume = {55},
	number = {6},
	year = {2001},
	note = {ISI Document Delivery No.: 503EQTimes Cited: 17Cited Reference Count: 15},
	pages = {585-589},
	type = {Article},
	abstract = {{The fixation reaction of copper-ethanolamine preservatives in wood was studied using the reaction between vanillin, a lignin model compound, and ethanolamine-copper sulphate solution. The green compound precipitated after the reaction has been characterized spectroscopically as di(ethanolamine)bis (vanillinato)dicopper(II); [Cu(vanillin) (ethanolamine)],. Single crystal X-ray crystallographic studies showed that the crystals of [Cu(vanillin)(ethanolamine)](2) are triclinic with the space group P1 with a = 9.1271(7)},
	keywords = {copper-ethanolamine, ESR, ethanolamine, FIXATION, LIGNIN MODEL COMPOUND, preservatives, VANILLIN, WOOD PRESERVATION, X-ray crystal structure},
	isbn = {0018-3830},
	url = {<Go to ISI>://000172786300005},
	author = {Ruddick, J. N. R. and Xie, C. S. and Herring, F. G.}
}
@article {4339,
	title = {The co-crystallization of Ru((R)-binap)(eta(3)-Me-allyl)(2) and binap dioxide, and synthesis of Ru(Ph2P(CH2)(4)PPh2)(eta(3)-Me-allyl)(2)},
	journal = {Journal of Organometallic Chemistry},
	volume = {557},
	number = {2},
	year = {1998},
	note = {ISI Document Delivery No.: ZQ872Times Cited: 8Cited Reference Count: 30},
	month = {Apr},
	pages = {213-219},
	type = {Article},
	abstract = {{The molecular structure of the 2-methylallyl species Ru((R)-binap)(eta(3)-Me-allyl)(2) (3) was established by X-ray crystallography of a crystal of 3a, the asymmetric unit of which is composed of half of a molecule of 3 and half of a (R)-(+)-2,2{\textquoteright}-bis(-diphenylphosphinoyl)-1,1{\textquoteright}-binaphthyl(binap dioxide) molecule, co-crystallized with two disordered deuterobenzenes; crystals of 3a are tetragonal, space group I422, with Z = 8},
	keywords = {allyl, ASYMMETRIC HYDROGENATION, BINAP, CATALYSTS, COMPLEXES, ENANTIOSELECTIVE HYDROGENATION, GENERAL-SYNTHESIS, KINETICS, rhodium, ruthenium, RUTHENIUM(II) COMPLEXES, X-ray crystal structure},
	isbn = {0022-328X},
	url = {<Go to ISI>://000073911500007},
	author = {Macfarlane, K. S. and Rettig, S. J. and Liu, Z. Q. and James, Brian R.}
}
@article {4003,
	title = {Stereoselective hydrogenation of lignin degradation model compounds},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {75},
	number = {9},
	year = {1997},
	note = {ISI Document Delivery No.: YE063Times Cited: 20Cited Reference Count: 29},
	month = {Sep},
	pages = {1234-1239},
	type = {Article},
	abstract = {Di-mu-chloro-bis(eta(4)-1,5-hexadiene)dirhodium(I) in a two-phase hexane-aqueous medium catalyzes the diastereoselective H-2-hydrogenation of lignin degradation model compounds 4-propylphenol, 2-methoxy-3-propylphenol, and 2,6-dimethoxy-3-propylphenol. The all-cis diastereomer is obtained selectively when the phenolic hydroxy group is protected as a methyl ether or when a model compound possessing two methoxy substituents adjacent to the phenolic hydroxy group is used. The relative stereochemistries of the hydrogenated products are established by X-ray crystal structure analysis and (or) H-1 NMR.},
	keywords = {catalytic hydrogenation, CATALYTIC-HYDROGENATION, COMPOUNDS, diastereomer, lignin degradation model, STEREOSELECTIVE, X-ray crystal structure},
	isbn = {0008-4042},
	url = {<Go to ISI>://A1997YE06300011},
	author = {Hu, Thomas Q. and James, Brian R. and Rettig, S. J. and Lee, C. L.}
}
@article {4003,
	title = {Stereoselective hydrogenation of lignin degradation model compounds},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {75},
	number = {9},
	year = {1997},
	note = {ISI Document Delivery No.: YE063Times Cited: 20Cited Reference Count: 29},
	month = {Sep},
	pages = {1234-1239},
	type = {Article},
	abstract = {Di-mu-chloro-bis(eta(4)-1,5-hexadiene)dirhodium(I) in a two-phase hexane-aqueous medium catalyzes the diastereoselective H-2-hydrogenation of lignin degradation model compounds 4-propylphenol, 2-methoxy-3-propylphenol, and 2,6-dimethoxy-3-propylphenol. The all-cis diastereomer is obtained selectively when the phenolic hydroxy group is protected as a methyl ether or when a model compound possessing two methoxy substituents adjacent to the phenolic hydroxy group is used. The relative stereochemistries of the hydrogenated products are established by X-ray crystal structure analysis and (or) H-1 NMR.},
	keywords = {catalytic hydrogenation, CATALYTIC-HYDROGENATION, COMPOUNDS, diastereomer, lignin degradation model, STEREOSELECTIVE, X-ray crystal structure},
	isbn = {0008-4042},
	url = {<Go to ISI>://A1997YE06300011},
	author = {Hu, Thomas Q. and James, Brian R. and Rettig, S. J. and Lee, C. L.}
}
@article {3568,
	title = {FIXATION OF AMMONIACAL COPPER PRESERVATIVES - REACTION OF VANILLIN, A LIGNIN MODEL-COMPOUND WITH AMMONIACAL COPPER-SULFATE SOLUTION},
	journal = {Holzforschung},
	volume = {49},
	number = {6},
	year = {1995},
	note = {ISI Document Delivery No.: TJ868Times Cited: 21Cited Reference Count: 23},
	pages = {483-490},
	type = {Article},
	abstract = {{A model for the fixation of ammoniacal copper preservatives in wood was examined through reaction of vanillin, a lignin model compound, with ammoniacal copper sulphate solution. The compound produced on evaporation of the aqueous ammoniacal solution has been characterized spectroscopically as di(amine)bis(vanillinato)copper(II); [Cu(vanillin)(2)(NH3)(2)]. Single crystal X-ray crystallographic studies showed that the crystals of [Cu(vanillin)(2)(NH3)(2)] are monoclinic with space group P2(1) with a = 5.4172(9)},
	keywords = {AMMONIACAL COPPER PRESERVATIVES, COMPLEXES, DIAMINE, ESR, FIXATION, ION, LIGNIN MODEL COMPOUND, RESONANCE, VANILLIN, WOOD PRESERVATION, X-ray crystal structure},
	isbn = {0018-3830},
	url = {<Go to ISI>://A1995TJ86800001},
	author = {Xie, C. S. and Ruddick, J. N. R. and Rettig, S. J. and Herring, F. G.}
}
