@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.}
}
@article {3678,
	title = {The ionic auxiliary concept in solid state organic photochemistry},
	journal = {Accounts of Chemical Research},
	volume = {29},
	number = {4},
	year = {1996},
	note = {ISI Document Delivery No.: UE738Times Cited: 121Cited Reference Count: 42},
	month = {Apr},
	pages = {203-209},
	type = {Review},
	keywords = {ASYMMETRIC INDUCTION, chirality, CRYSTAL, KETONES, PHOTOREARRANGEMENT, REACTIVITY, SALTS, SUPRAMOLECULAR PHOTOCHEMISTRY},
	isbn = {0001-4842},
	url = {<Go to ISI>://A1996UE73800006},
	author = {Gamlin, J. N. and Jones, R. and Leibovitch, M. and Patrick, B. and Scheffer, J. R. and Trotter, J.}
}
@article {3678,
	title = {The ionic auxiliary concept in solid state organic photochemistry},
	journal = {Accounts of Chemical Research},
	volume = {29},
	number = {4},
	year = {1996},
	note = {ISI Document Delivery No.: UE738Times Cited: 121Cited Reference Count: 42},
	month = {Apr},
	pages = {203-209},
	type = {Review},
	keywords = {ASYMMETRIC INDUCTION, chirality, CRYSTAL, KETONES, PHOTOREARRANGEMENT, REACTIVITY, SALTS, SUPRAMOLECULAR PHOTOCHEMISTRY},
	isbn = {0001-4842},
	url = {<Go to ISI>://A1996UE73800006},
	author = {Gamlin, J. N. and Jones, R. and Leibovitch, M. and Patrick, B. and Scheffer, J. R. and Trotter, J.}
}
