@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.}
}
