@article {3366,
	title = {CONTROL OF THE SOLID-STATE PHOTODIMERIZATION OF SOME DERIVATIVES AND ANALOGS OF TRANS-CINNAMIC ACID BY ETHYLENEDIAMINE},
	journal = {Tetrahedron Letters},
	volume = {36},
	number = {34},
	year = {1995},
	note = {ISI Document Delivery No.: RR016Times Cited: 39Cited Reference Count: 9},
	month = {Aug},
	pages = {6087-6090},
	type = {Article},
	abstract = {Some of double salts derived from ethylenediamine (en) and a variety of trans-cinnamic acids and their analogs underwent photodimerization in the solid state, giving predominantly beta-truxinic dimers. X-Ray studies demonstrate that (a) the conformation of en is gauche for the highly photoreactive double salts (o-1b . en and m-1e . en), whereas it is anti for less photoreactive o-1a . en or photoinert 1d . en and (b) for highly reactive o-1b . en and m-1e . en, the monomer acid molecules are arranged in an overlap configuration and a reactive monomer pair is hydrogen-bonded to the same en molecule.},
	isbn = {0040-4039},
	url = {<Go to ISI>://A1995RR01600024},
	author = {Ito, Y. and Borecka, B. and Olovsson, G. and Trotter, J. and Scheffer, J. R.}
}
