@article {7346,
	title = {SELECTIVE SOLID-STATE PHOTOREARRANGEMENT THROUGH THE LESS STABLE OF 2 POSSIBLE BIRADICAL INTERMEDIATES},
	journal = {Journal of Organic Chemistry},
	volume = {57},
	number = {5},
	year = {1992},
	note = {ISI Document Delivery No.: HG741Times Cited: 12Cited Reference Count: 32},
	month = {Feb},
	pages = {1486-1494},
	type = {Article},
	abstract = {The photochemistry of methyl 2-benzoyl-1,4-dihydro-1,4-ethenonaphthalene-3-carboxylate is completely medium-dependent. In solution, two primary di-pi-methane-type photoproducts are formed. Neither of these products is produced when the photolysis is carried out in the solid state; instead, three new photoproducts are formed. The results are interpreted as being due to reaction through 1,3-biradical intermediates, the more stable of which are preferred in solution whereas the less stable ones are formed in the solid state as a result of topochemical restrictions of molecular motion. X-ray crystallographic evidence in support of these ideas is presented and discussed.},
	keywords = {CRYSTALS, EXPLORATORY ORGANIC-PHOTOCHEMISTRY, HYDROGEN ABSTRACTION REACTIONS, POLAR SUBSTITUENTS, REARRANGEMENT},
	isbn = {0022-3263},
	url = {<Go to ISI>://A1992HG74100030},
	author = {Pokkuluri, P. R. and Scheffer, J. R. and Trotter, J. and Yap, M.}
}
@article {7346,
	title = {SELECTIVE SOLID-STATE PHOTOREARRANGEMENT THROUGH THE LESS STABLE OF 2 POSSIBLE BIRADICAL INTERMEDIATES},
	journal = {Journal of Organic Chemistry},
	volume = {57},
	number = {5},
	year = {1992},
	note = {ISI Document Delivery No.: HG741Times Cited: 12Cited Reference Count: 32},
	month = {Feb},
	pages = {1486-1494},
	type = {Article},
	abstract = {The photochemistry of methyl 2-benzoyl-1,4-dihydro-1,4-ethenonaphthalene-3-carboxylate is completely medium-dependent. In solution, two primary di-pi-methane-type photoproducts are formed. Neither of these products is produced when the photolysis is carried out in the solid state; instead, three new photoproducts are formed. The results are interpreted as being due to reaction through 1,3-biradical intermediates, the more stable of which are preferred in solution whereas the less stable ones are formed in the solid state as a result of topochemical restrictions of molecular motion. X-ray crystallographic evidence in support of these ideas is presented and discussed.},
	keywords = {CRYSTALS, EXPLORATORY ORGANIC-PHOTOCHEMISTRY, HYDROGEN ABSTRACTION REACTIONS, POLAR SUBSTITUENTS, REARRANGEMENT},
	isbn = {0022-3263},
	url = {<Go to ISI>://A1992HG74100030},
	author = {Pokkuluri, P. R. and Scheffer, J. R. and Trotter, J. and Yap, M.}
}
