@article {2557,
	title = {10-Ethynyl-2,3,6,6a,9,10-hexahydro-1H-6,9-methanopyrrolo[2,1-i][2,1]benz othiazol-10-ol 5,5-dioxide},
	journal = {Acta Crystallographica Section E-Structure Reports Online},
	volume = {65},
	year = {2009},
	note = {ISI Document Delivery No.: 521FUTimes Cited: 0Cited Reference Count: 7Patrick, B. O. Liang, H. Canesi, S. Ciufolini, M. A.Part 11},
	month = {Nov},
	pages = {O2621-U2491},
	type = {Article},
	abstract = {In the title compound, C13H15NO3S, the sole classical hydrogen-bond donor is involved in an intramolecular O-H center dot center dot center dot N hydrogen bond. In the crystal structure, pairs of molecules related by inversion centres are linked by pairs of weak intermolecular C-H center dot center dot center dot O interactions; these centrosymmetric pairs are, in turn, linked further by weak intermolecular C-H center dot center dot center dot O interactions, forming two-dimensional sheets oriented parallel to (101).},
	keywords = {OXIDATIVE AMIDATION, PHENOLS},
	isbn = {1600-5368},
	url = {<Go to ISI>://000271906600206},
	author = {Patrick, B. O. and Liang, H. and Canesi, S. and Ciufolini,Marco A.}
}
@article {2505,
	title = {Crystal structure of 2,3,6a,9-tetrahydro-1H-6,9-methanopyrrolo[2,1-i][2,1]benzisothiazol-10(6 H)-one 5,5-dioxide, C11H13NO3S},
	journal = {Zeitschrift Fur Kristallographie-New Crystal Structures},
	volume = {224},
	number = {1},
	year = {2009},
	note = {ISI Document Delivery No.: 435PATimes Cited: 2Cited Reference Count: 6Liang, Huan Canesi, Sylvain Patrick, Brian O. Ciufolini, Marco A.},
	pages = {83-84},
	type = {Article},
	abstract = {{C11H13NO3S, monoclinic, P12(1)/c1 (no. 14)},
	keywords = {OXIDATIVE AMIDATION, PHENOLS},
	isbn = {1433-7266},
	url = {<Go to ISI>://000265354600037},
	author = {Liang, H. and Canesi, S. and Patrick, B. O. and Ciufolini,Marco A.}
}
@article {2530,
	title = {Oxidation of Oximes to Nitrile Oxides with Hypervalent Iodine Reagents},
	journal = {Organic Letters},
	volume = {11},
	number = {7},
	year = {2009},
	note = {ISI Document Delivery No.: 425FOTimes Cited: 21Cited Reference Count: 33Mendelsohn, Brian A. Lee, Shelley Kim, Simon Teyssier, Florian Aulakh, Virender S. Ciufolini, Marco A.},
	month = {Apr},
	pages = {1539-1542},
	type = {Article},
	abstract = {Iodobenzene diacetate in MeOH containing a catalytic amount of TFA efficiently oxidizes aldoximes to nitrile oxides. The latter may be trapped in situ with olefins in a bimolecular or an intramolecular mode. The new method enables the execution of tandem oxidative dearomatization of phenols/intramolecular nitrile oxide cycloaddition sequences leading to useful synthetic intermediates.},
	keywords = {AMIDATION, CARBONYL-COMPOUNDS, CHEMISTRY, CONVERSION, DESS-MARTIN PERIODINANE, DIRECTIONS, FR901483, PHENOLS, TOSYLATES, TOSYLHYDRAZONES},
	isbn = {1523-7060},
	url = {<Go to ISI>://000264622600020},
	author = {Mendelsohn, B. A. and Lee, S. and Kim, S. and Teyssier, F. and Aulakh, V. S. and Ciufolini,Marco A.}
}
@article {5136,
	title = {Tetrazole ethers from lignin model phenols: synthesis, crystal structures, and photostability},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {79},
	number = {8},
	year = {2001},
	note = {ISI Document Delivery No.: 473WGTimes Cited: 1Cited Reference Count: 24},
	month = {Aug},
	pages = {1201-1206},
	type = {Article},
	abstract = {{The phenolic OH moiety in lignin is one of the key functional groups responsible for the photo-induced yellowing of mechanical wood pulps and papers. To evaluate new protective groups for the stabilization of lignin phenols, the model compounds, 2-methoxy-4-propylphenol (1) and 4-hydroxy-3-methoxyacetophenone (2) were reacted with 5-chloro-1-phenyl-1H-tetrazole to give the corresponding tetrazole ethers 1{\textquoteright} and 2{\textquoteright}, respectively, that were then studied for their photostability. The synthesis of these ethers was more efficient than that of alkyl ethers because of less hydrolysis of the alkylating agent under the reaction conditions. Compounds 1{\textquoteright} and 2{\textquoteright} were fully characterized, including X-ray crystal structure analyses. Crystals of 1{\textquoteright} and 2{\textquoteright} were monoclinic of space groups P2(1)/c and P2(1)/a, respectively. For 1{\textquoteright}: a = 9.8679(6)},
	keywords = {ALKYLATION, ETHERS, HIGH-YIELD PULPS, LIGHT, LIGNIN MODEL COMPOUNDS, METHYLATION, PHENOLS, yellowing inhibition},
	isbn = {0008-4042},
	url = {<Go to ISI>://000171071400001},
	author = {Lu, A. Z. and Hu, Thomas Q. and Osmond, D. A. and Patrick, B. O. and James, Brian R.}
}
@article {5136,
	title = {Tetrazole ethers from lignin model phenols: synthesis, crystal structures, and photostability},
	journal = {Canadian Journal of Chemistry-Revue Canadienne De Chimie},
	volume = {79},
	number = {8},
	year = {2001},
	note = {ISI Document Delivery No.: 473WGTimes Cited: 1Cited Reference Count: 24},
	month = {Aug},
	pages = {1201-1206},
	type = {Article},
	abstract = {{The phenolic OH moiety in lignin is one of the key functional groups responsible for the photo-induced yellowing of mechanical wood pulps and papers. To evaluate new protective groups for the stabilization of lignin phenols, the model compounds, 2-methoxy-4-propylphenol (1) and 4-hydroxy-3-methoxyacetophenone (2) were reacted with 5-chloro-1-phenyl-1H-tetrazole to give the corresponding tetrazole ethers 1{\textquoteright} and 2{\textquoteright}, respectively, that were then studied for their photostability. The synthesis of these ethers was more efficient than that of alkyl ethers because of less hydrolysis of the alkylating agent under the reaction conditions. Compounds 1{\textquoteright} and 2{\textquoteright} were fully characterized, including X-ray crystal structure analyses. Crystals of 1{\textquoteright} and 2{\textquoteright} were monoclinic of space groups P2(1)/c and P2(1)/a, respectively. For 1{\textquoteright}: a = 9.8679(6)},
	keywords = {ALKYLATION, ETHERS, HIGH-YIELD PULPS, LIGHT, LIGNIN MODEL COMPOUNDS, METHYLATION, PHENOLS, yellowing inhibition},
	isbn = {0008-4042},
	url = {<Go to ISI>://000171071400001},
	author = {Lu, A. Z. and Hu, Thomas Q. and Osmond, D. A. and Patrick, B. O. and James, Brian R.}
}
