@article {2510,
	title = {The Engineering of Bacteria Bearing Azido-Pseudaminic Acid-Modified Flagella},
	journal = {Chembiochem},
	volume = {10},
	number = {8},
	year = {2009},
	note = {ISI Document Delivery No.: 452SMTimes Cited: 3Cited Reference Count: 24Liu, Feng Aubry, Annie J. Schoenhofen, Ian C. Logan, Susan M. Tanner, Martin E.},
	month = {May},
	pages = {1317-1320},
	type = {Article},
	keywords = {4, 6-DEHYDRATASE, azides, biosynthesis, C. jejuni, CAMPYLOBACTER-JEJUNI, cell surfaces, flagella, FUNCTIONAL-CHARACTERIZATION, HELICOBACTER-PYLORI, IDENTIFICATION, METABOLISM, PATHWAY, PROTEINS, PseB, reaction, Staudinger, UDP-N-ACETYLGLUCOSAMINE},
	isbn = {1439-4227},
	url = {<Go to ISI>://000266561500009},
	author = {Liu, F. and Aubry, A. J. and Schoenhofen, I. C. and Logan, S. M. and Tanner, M. E.}
}
@article {966,
	title = {The mechanism of the reaction catalyzed by ADP-beta-L-glycero-D-manno-heptose 6-epimerase},
	journal = {Journal of the American Chemical Society},
	volume = {126},
	number = {29},
	year = {2004},
	note = {ISI Document Delivery No.: 840JTTimes Cited: 14Cited Reference Count: 24},
	month = {Jul},
	pages = {8878-8879},
	type = {Article},
	keywords = {4, 6-DEHYDRATASE, BACTERIA, D-MANNOHEPTOSE 6-EPIMERASE, EPIMERIZATION, ESCHERICHIA-COLI, GLUCOSE, INSIGHTS, NUCLEOTIDE-MODIFYING ENZYMES, OUTER-MEMBRANE, UDP-GALACTOSE 4-EPIMERASE},
	isbn = {0002-7863},
	url = {<Go to ISI>://000222855300009},
	author = {Read, J. A. and Ahmed, R. A. and Morrison, J. P. and Coleman, W. G. and Tanner, M. E.}
}
@article {5208,
	title = {Sugar nucleotide-modifying enzymes},
	journal = {Current Organic Chemistry},
	volume = {5},
	number = {2},
	year = {2001},
	note = {ISI Document Delivery No.: 411FKTimes Cited: 12Cited Reference Count: 170},
	month = {Feb},
	pages = {169-192},
	type = {Review},
	abstract = {Sugar nucleotides serve as the activated forms of carbohydrates that are used in a wide range of biosynthetic pathways. Instead of building up the sugar nucleotide from the free sugar itself, nature often chooses to modify the "donor" portion of a pre-existing sugar nucleotide in a biosynthetically efficient manner. In doing so a rich variety of catalytic strategies are employed and this review focuses on recent mechanistic and structural studies of the sugar nucleotide-modifying enzymes. The review is organized around the types of reactions catalyzed and contains the following sections: Epimerases/Mutases/Decarboxylases, Eliminations and Substitutions, Oxidation and Reduction, and Substitutions on the Periphery of Sugar Nucleotides.},
	keywords = {4, 6-DEHYDRATASE, 6-DIDEOXYHEXOSES, ACETYLGLUCOSAMINE 2-EPIMERASE/N-ACETYLMANNOSAMINE, ACETYLNEURAMINIC ACID, biosynthesis, CYTIDINE DIPHOSPHATE 3, D-GLUCOSE, ESCHERICHIA-COLI K-12, FIRST 2, GDP-FUCOSE SYNTHETASE, KINASE, N-ACETYLGLUCOSAMINE, SITE-DIRECTED MUTAGENESIS, STEPS, UDP-GALACTOSE 4-EPIMERASE},
	isbn = {1385-2728},
	url = {<Go to ISI>://000167487300004},
	author = {Tanner, M. E.}
}
@article {3974,
	title = {4-[2,4,6-tris(1-methylethyl)benzoyl]benzoic acid (S)-(-)-proline},
	journal = {Acta Crystallographica Section C-Crystal Structure Communications},
	volume = {53},
	year = {1997},
	note = {ISI Document Delivery No.: XZ627Times Cited: 2Cited Reference Count: 13Part 9},
	month = {Sep},
	pages = {1259-1262},
	type = {Article},
	abstract = {The title compound, C23H28O3.C5H9NO2, is a 1:1 complex of the benzoic acid derivative and the (S)-proline zwitterion, with two formula units in the asymmetric unit (with pseudo-symmetry relationships between the separate components). The ketone carbonyl group in each benzoic acid molecule deviates slightly from a position normal to the plane of the triisopropylphenyl ring; the deviations (of about 16 degrees) are in opposite senses in the two molecules, so that the molecules have opposite conformational chiralities, leading to a nearly racemic photoproduct on solid-state photolysis.},
	keywords = {2, 4, 6-TRIISOPROPYLBENZOPHENONES, CRYSTAL-STRUCTURES, SOLID-STATE PHOTOCHEMISTRY},
	isbn = {0108-2701},
	url = {<Go to ISI>://A1997XZ62700042},
	author = {Fu, T. Y. and Scheffer, J. R. and Trotter, J.}
}
@article {3974,
	title = {4-[2,4,6-tris(1-methylethyl)benzoyl]benzoic acid (S)-(-)-proline},
	journal = {Acta Crystallographica Section C-Crystal Structure Communications},
	volume = {53},
	year = {1997},
	note = {ISI Document Delivery No.: XZ627Times Cited: 2Cited Reference Count: 13Part 9},
	month = {Sep},
	pages = {1259-1262},
	type = {Article},
	abstract = {The title compound, C23H28O3.C5H9NO2, is a 1:1 complex of the benzoic acid derivative and the (S)-proline zwitterion, with two formula units in the asymmetric unit (with pseudo-symmetry relationships between the separate components). The ketone carbonyl group in each benzoic acid molecule deviates slightly from a position normal to the plane of the triisopropylphenyl ring; the deviations (of about 16 degrees) are in opposite senses in the two molecules, so that the molecules have opposite conformational chiralities, leading to a nearly racemic photoproduct on solid-state photolysis.},
	keywords = {2, 4, 6-TRIISOPROPYLBENZOPHENONES, CRYSTAL-STRUCTURES, SOLID-STATE PHOTOCHEMISTRY},
	isbn = {0108-2701},
	url = {<Go to ISI>://A1997XZ62700042},
	author = {Fu, T. Y. and Scheffer, J. R. and Trotter, J.}
}
@article {3675,
	title = {Crystal structure-reactivity relationships in the solid state photochemistry of 2,4,6-triisopropylthiobenzophenone: C=O...H versus C=S...H abstraction geometry},
	journal = {Tetrahedron Letters},
	volume = {37},
	number = {13},
	year = {1996},
	note = {ISI Document Delivery No.: UC590Times Cited: 6Cited Reference Count: 19},
	month = {Mar},
	pages = {2125-2128},
	type = {Article},
	abstract = {X-ray crystal structure solid state photoreactivity correlations are reported for 2,4,6-triisopropylthiobenzophenone (1a) and its p-methoxy derivative 1b. The results reveal interesting differences in the geometry of gamma-hydrogen atom abstraction for ketones and thiones.},
	keywords = {2, 4, 6-TRIISOPROPYLBENZOPHENONES, CONFORMATION, KETONES, PHOTOCYCLIZATION, TRIPLET-STATES},
	isbn = {0040-4039},
	url = {<Go to ISI>://A1996UC59000003},
	author = {Fu, T. Y. and Scheffer, J. R. and Trotter, J.}
}
@article {3675,
	title = {Crystal structure-reactivity relationships in the solid state photochemistry of 2,4,6-triisopropylthiobenzophenone: C=O...H versus C=S...H abstraction geometry},
	journal = {Tetrahedron Letters},
	volume = {37},
	number = {13},
	year = {1996},
	note = {ISI Document Delivery No.: UC590Times Cited: 6Cited Reference Count: 19},
	month = {Mar},
	pages = {2125-2128},
	type = {Article},
	abstract = {X-ray crystal structure solid state photoreactivity correlations are reported for 2,4,6-triisopropylthiobenzophenone (1a) and its p-methoxy derivative 1b. The results reveal interesting differences in the geometry of gamma-hydrogen atom abstraction for ketones and thiones.},
	keywords = {2, 4, 6-TRIISOPROPYLBENZOPHENONES, CONFORMATION, KETONES, PHOTOCYCLIZATION, TRIPLET-STATES},
	isbn = {0040-4039},
	url = {<Go to ISI>://A1996UC59000003},
	author = {Fu, T. Y. and Scheffer, J. R. and Trotter, J.}
}
@article {3520,
	title = {CARCEPLEXES AND HEMICARCEPLEXES - MOLECULAR ENCAPSULATION - FROM HOURS TO FOREVER},
	journal = {Tetrahedron},
	volume = {51},
	number = {12},
	year = {1995},
	note = {ISI Document Delivery No.: QN982Times Cited: 70Cited Reference Count: 124},
	month = {Mar},
	pages = {3395-3422},
	type = {Review},
	keywords = {4, CARBON NANOTUBES, CARCERANDS, CAVITANDS, CHEMISTRY, CONSTRICTIVE BINDING, CONTAINER COMPOUNDS, HEMICARCERANDS, HOST-GUEST COMPLEXATION, PORTALS, SHELL CLOSURE, supramolecular},
	isbn = {0040-4020},
	url = {<Go to ISI>://A1995QN98200001},
	author = {Sherman, J. C.}
}
@article {3082,
	title = {IONIC CHIRAL HANDLE-INDUCED ASYMMETRIC-SYNTHESIS IN A SOLID-STATE NORRISH TYPE-II PHOTOREACTION},
	journal = {Tetrahedron-Asymmetry},
	volume = {5},
	number = {8},
	year = {1994},
	note = {ISI Document Delivery No.: PC678Times Cited: 22Cited Reference Count: 9},
	month = {Aug},
	pages = {1415-1418},
	type = {Article},
	abstract = {Irradiation of crystals of salts formed between 4-(2,4,6-triisopropylbenzoyl)benzoic acid (1a) and various optically active amines is shown to lead to optically active Norrish type II photoproducts in low to moderate enantiomeric excesses, a process in which the ammonium ion has acted as an {\textquoteright}{\textquoteright}ionic chiral handle.{\textquoteright}{\textquoteright} X-ray crystallography reveals that the salts crystallize with two independent, mirror image-related molecules of the benzophenone moiety in the asymmetric unit, and this is suggested to be the source of the low ees observed.},
	keywords = {2, 4, 6-TRIISOPROPYLBENZOPHENONES, INDUCTION, PHOTOCHEMISTRY, SALTS},
	isbn = {0957-4166},
	url = {<Go to ISI>://A1994PC67800004},
	author = {Koshima, H. and Maeda, A. and Masuda, N. and Matsuura, T. and Hirotsu, K. and Okada, K. and Mizutari, H. and Ito, Y. and Fu, T. Y. and Scheffer, J. R. and Trotter, J.}
}
@article {3082,
	title = {IONIC CHIRAL HANDLE-INDUCED ASYMMETRIC-SYNTHESIS IN A SOLID-STATE NORRISH TYPE-II PHOTOREACTION},
	journal = {Tetrahedron-Asymmetry},
	volume = {5},
	number = {8},
	year = {1994},
	note = {ISI Document Delivery No.: PC678Times Cited: 22Cited Reference Count: 9},
	month = {Aug},
	pages = {1415-1418},
	type = {Article},
	abstract = {Irradiation of crystals of salts formed between 4-(2,4,6-triisopropylbenzoyl)benzoic acid (1a) and various optically active amines is shown to lead to optically active Norrish type II photoproducts in low to moderate enantiomeric excesses, a process in which the ammonium ion has acted as an {\textquoteright}{\textquoteright}ionic chiral handle.{\textquoteright}{\textquoteright} X-ray crystallography reveals that the salts crystallize with two independent, mirror image-related molecules of the benzophenone moiety in the asymmetric unit, and this is suggested to be the source of the low ees observed.},
	keywords = {2, 4, 6-TRIISOPROPYLBENZOPHENONES, INDUCTION, PHOTOCHEMISTRY, SALTS},
	isbn = {0957-4166},
	url = {<Go to ISI>://A1994PC67800004},
	author = {Koshima, H. and Maeda, A. and Masuda, N. and Matsuura, T. and Hirotsu, K. and Okada, K. and Mizutari, H. and Ito, Y. and Fu, T. Y. and Scheffer, J. R. and Trotter, J.}
}
