@article {4506,
	title = {Linearly conjugated benzocyclohexadienone photochemistry in the solid state: ionic chiral auxiliary mediated asymmetric induction},
	journal = {Tetrahedron Letters},
	volume = {40},
	number = {50},
	year = {1999},
	note = {ISI Document Delivery No.: 258FJTimes Cited: 16Cited Reference Count: 3},
	month = {Dec},
	pages = {8737-8740},
	type = {Article},
	abstract = {Asymmetric induction in the photochemistry of a linearly conjugated benzocyclohexadienone derivative has been achieved for the first time through the use of the solid state ionic chiral auxiliary method. Enantiomeric excesses as high as 70-80\% at reasonable conversions are readily attainable. Crystal structures for both reactant and product are reported. (C) 1999 Elsevier Science Ltd. All rights reserved.},
	keywords = {ASYMMETRIC INDUCTION, KETONES, PHOTOCHEMISTRY, REARRANGEMENT, [pi(a)(2)+sigma(a)(2)]},
	isbn = {0040-4039},
	url = {<Go to ISI>://000083827200005},
	author = {Cheung, E. and Netherton, M. R. and Scheffer, J. R. and Trotter, J.}
}
@article {4506,
	title = {Linearly conjugated benzocyclohexadienone photochemistry in the solid state: ionic chiral auxiliary mediated asymmetric induction},
	journal = {Tetrahedron Letters},
	volume = {40},
	number = {50},
	year = {1999},
	note = {ISI Document Delivery No.: 258FJTimes Cited: 16Cited Reference Count: 3},
	month = {Dec},
	pages = {8737-8740},
	type = {Article},
	abstract = {Asymmetric induction in the photochemistry of a linearly conjugated benzocyclohexadienone derivative has been achieved for the first time through the use of the solid state ionic chiral auxiliary method. Enantiomeric excesses as high as 70-80\% at reasonable conversions are readily attainable. Crystal structures for both reactant and product are reported. (C) 1999 Elsevier Science Ltd. All rights reserved.},
	keywords = {ASYMMETRIC INDUCTION, KETONES, PHOTOCHEMISTRY, REARRANGEMENT, [pi(a)(2)+sigma(a)(2)]},
	isbn = {0040-4039},
	url = {<Go to ISI>://000083827200005},
	author = {Cheung, E. and Netherton, M. R. and Scheffer, J. R. and Trotter, J.}
}
