@article {4762,
	title = {Conformational enantiomerism in chiral organic salts containing crystallographically independent anion-cation pairs},
	journal = {Journal of the American Chemical Society},
	volume = {122},
	number = {47},
	year = {2000},
	note = {ISI Document Delivery No.: 380HYTimes Cited: 17Cited Reference Count: 15},
	month = {Nov},
	pages = {11753-11754},
	type = {Article},
	keywords = {asymmetric, CARBOXYLATE, INDUCTION, SOLID-STATE PHOTOCHEMISTRY, YANG PHOTOCYCLIZATION REACTION},
	isbn = {0002-7863},
	url = {<Go to ISI>://000165696800029},
	author = {Cheung, E. and Kang, T. and Netherton, M. R. and Scheffer, J. R. and Trotter, J.}
}
@article {4762,
	title = {Conformational enantiomerism in chiral organic salts containing crystallographically independent anion-cation pairs},
	journal = {Journal of the American Chemical Society},
	volume = {122},
	number = {47},
	year = {2000},
	note = {ISI Document Delivery No.: 380HYTimes Cited: 17Cited Reference Count: 15},
	month = {Nov},
	pages = {11753-11754},
	type = {Article},
	keywords = {asymmetric, CARBOXYLATE, INDUCTION, SOLID-STATE PHOTOCHEMISTRY, YANG PHOTOCYCLIZATION REACTION},
	isbn = {0002-7863},
	url = {<Go to ISI>://000165696800029},
	author = {Cheung, E. and Kang, T. and Netherton, M. R. and Scheffer, J. R. and Trotter, J.}
}
@article {4508,
	title = {Asymmetric induction in the solid state photochemistry of an alpha-mesitylacetophenone derivative through the use of ionic chiral auxiliaries},
	journal = {Tetrahedron Letters},
	volume = {40},
	number = {50},
	year = {1999},
	note = {ISI Document Delivery No.: 258FJTimes Cited: 15Cited Reference Count: 8},
	month = {Dec},
	pages = {8733-8736},
	type = {Article},
	abstract = {Irradiation in the crystalline state of salts formed between alpha-mesitylacetophenone-p-carboxylic acid and a variety of optically pure amines - the so-called {\textquoteright}ionic chiral auxiliary{\textquoteright} approach to asymmetric synthesis - leads to the corresponding 2-indanol in excellent yield and in high enantiomeric excess. X-Ray crystallography reveals the source of the enantioselectivity. (C) 1999 Elsevier Science Ltd. All rights reserved.},
	keywords = {ASYMMETRIC INDUCTION, CARBOXYLATE, CRYSTAL, KETONES, PHOTOCHEMISTRY, REARRANGEMENTS},
	isbn = {0040-4039},
	url = {<Go to ISI>://000083827200004},
	author = {Cheung, E. and Rademacher, K. and Scheffer, J. R. and Trotter, J.}
}
@article {4508,
	title = {Asymmetric induction in the solid state photochemistry of an alpha-mesitylacetophenone derivative through the use of ionic chiral auxiliaries},
	journal = {Tetrahedron Letters},
	volume = {40},
	number = {50},
	year = {1999},
	note = {ISI Document Delivery No.: 258FJTimes Cited: 15Cited Reference Count: 8},
	month = {Dec},
	pages = {8733-8736},
	type = {Article},
	abstract = {Irradiation in the crystalline state of salts formed between alpha-mesitylacetophenone-p-carboxylic acid and a variety of optically pure amines - the so-called {\textquoteright}ionic chiral auxiliary{\textquoteright} approach to asymmetric synthesis - leads to the corresponding 2-indanol in excellent yield and in high enantiomeric excess. X-Ray crystallography reveals the source of the enantioselectivity. (C) 1999 Elsevier Science Ltd. All rights reserved.},
	keywords = {ASYMMETRIC INDUCTION, CARBOXYLATE, CRYSTAL, KETONES, PHOTOCHEMISTRY, REARRANGEMENTS},
	isbn = {0040-4039},
	url = {<Go to ISI>://000083827200004},
	author = {Cheung, E. and Rademacher, K. and Scheffer, J. R. and Trotter, J.}
}
@article {4505,
	title = {An ionic chiral auxiliary-induced regioselective and enantioselective Yang photocyclization reaction in the crystalline state},
	journal = {Tetrahedron Letters},
	volume = {40},
	number = {50},
	year = {1999},
	note = {ISI Document Delivery No.: 258FJTimes Cited: 16Cited Reference Count: 19},
	month = {Dec},
	pages = {8729-8732},
	type = {Article},
	abstract = {cis-9-Decalyl aryl ketones undergo Yang photocyclization in solution to afford an approximately 1:1 mixture of two regioisomeric racemic cyclobutanols. In contrast, irradiation in the crystalline state in the presence of various ionic chiral auxiliaries leads to a single cyclobutanol in >98\% enantiomeric excess. X-Ray crystallography reveals the source of the regio-, diastereo- and enantioselectivity. (C) 1999 Elsevier Science Ltd. All rights reserved.},
	keywords = {ASYMMETRIC INDUCTION, CARBOXYLATE, KETONES, ORGANIC-PHOTOCHEMISTRY, PHOTOCHEMISTRY, SOLID-STATE, Yang photocyclization},
	isbn = {0040-4039},
	url = {<Go to ISI>://000083827200003},
	author = {Cheung, E. and Kang, T. and Raymond, J. R. and Scheffer, J. R. and Trotter, J.}
}
@article {4505,
	title = {An ionic chiral auxiliary-induced regioselective and enantioselective Yang photocyclization reaction in the crystalline state},
	journal = {Tetrahedron Letters},
	volume = {40},
	number = {50},
	year = {1999},
	note = {ISI Document Delivery No.: 258FJTimes Cited: 16Cited Reference Count: 19},
	month = {Dec},
	pages = {8729-8732},
	type = {Article},
	abstract = {cis-9-Decalyl aryl ketones undergo Yang photocyclization in solution to afford an approximately 1:1 mixture of two regioisomeric racemic cyclobutanols. In contrast, irradiation in the crystalline state in the presence of various ionic chiral auxiliaries leads to a single cyclobutanol in >98\% enantiomeric excess. X-Ray crystallography reveals the source of the regio-, diastereo- and enantioselectivity. (C) 1999 Elsevier Science Ltd. All rights reserved.},
	keywords = {ASYMMETRIC INDUCTION, CARBOXYLATE, KETONES, ORGANIC-PHOTOCHEMISTRY, PHOTOCHEMISTRY, SOLID-STATE, Yang photocyclization},
	isbn = {0040-4039},
	url = {<Go to ISI>://000083827200003},
	author = {Cheung, E. and Kang, T. and Raymond, J. R. and Scheffer, J. R. and Trotter, J.}
}
@article {4053,
	title = {Absolute configuration correlation studies in solid state organic photochemistry},
	journal = {Pure and Applied Chemistry},
	volume = {69},
	number = {4},
	year = {1997},
	note = {ISI Document Delivery No.: XH296Times Cited: 30Cited Reference Count: 1716th IUPAC Symposium on PhotochemistryJUL 21-26, 1996HELSINKI, FINLANDIUPAC},
	month = {Apr},
	pages = {815-823},
	type = {Proceedings Paper},
	abstract = {An ever-increasing number of examples in the literature attest to the fact that photochemical reactions carried out in optically active crystalline media can lead to enantiomerically enriched products in high optical yields. Taken from our own work and that of others, this article examines the relatively few examples of such reactions in which the absolute stereochemical arrangements of the molecules in the reactant crystals are correlated with the absolute configurations of the optically active products formed by irradiation of the same crystals. Studies of this type provide penetrating insights into the mechanisms of the reactions in question, and in addition, help to pinpoint the crystal lattice-derived stereoelectronic factors that an responsible for the observed enantioselectivities.},
	keywords = {CARBOXYLATE, CRYSTAL, PHOTOREARRANGEMENT, SUPRAMOLECULAR PHOTOCHEMISTRY},
	isbn = {0033-4545},
	url = {<Go to ISI>://A1997XH29600027},
	author = {Leibovitch, M. and Olovsson, G. and Scheffer, J. R. and Trotter, J.}
}
@article {4053,
	title = {Absolute configuration correlation studies in solid state organic photochemistry},
	journal = {Pure and Applied Chemistry},
	volume = {69},
	number = {4},
	year = {1997},
	note = {ISI Document Delivery No.: XH296Times Cited: 30Cited Reference Count: 1716th IUPAC Symposium on PhotochemistryJUL 21-26, 1996HELSINKI, FINLANDIUPAC},
	month = {Apr},
	pages = {815-823},
	type = {Proceedings Paper},
	abstract = {An ever-increasing number of examples in the literature attest to the fact that photochemical reactions carried out in optically active crystalline media can lead to enantiomerically enriched products in high optical yields. Taken from our own work and that of others, this article examines the relatively few examples of such reactions in which the absolute stereochemical arrangements of the molecules in the reactant crystals are correlated with the absolute configurations of the optically active products formed by irradiation of the same crystals. Studies of this type provide penetrating insights into the mechanisms of the reactions in question, and in addition, help to pinpoint the crystal lattice-derived stereoelectronic factors that an responsible for the observed enantioselectivities.},
	keywords = {CARBOXYLATE, CRYSTAL, PHOTOREARRANGEMENT, SUPRAMOLECULAR PHOTOCHEMISTRY},
	isbn = {0033-4545},
	url = {<Go to ISI>://A1997XH29600027},
	author = {Leibovitch, M. and Olovsson, G. and Scheffer, J. R. and Trotter, J.}
}
