@article { ISI:000230879600018,
	title = {Stereoselectivity ratios in a simple Diels-Alder reaction in aqueous salt solutions of alcohols},
	journal = {Tetrahedron},
	volume = {61},
	number = {33},
	year = {2005},
	month = {AUG},
	pages = {8025-8030},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	type = {Article},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>This is the first exhaustive report on the variation of stereoselectivity ratios for a simple Diels-Alder reaction between cyclopentadiene and methyl acrylate. The reaction was carried out in aqueous mixtures of methanol, ethanol, propan-1-ol and butan-1-ol in presence of LiClO4, LiCl, NaCl, KCl, CaCl2 and MgCl2. The endo sterecisomer decreases with the increase in carbon chain length of the alcohol. However, LiClO4, a salting-in agent in water becomes salting-out in aqueous mixtures of alcohols. The solvent properties, thus can be attuned by adjusting the amount of solvents and salts. (c) 2005 Elsevier Ltd. All rights reserved.</p>},
	keywords = {aqueous alcohols, Diels-Alder reaction, endolexo ratios, salts},
	issn = {0040-4020},
	doi = {10.1016/j.tet.2005.06.010},
	author = {Deshpande, Suvarna S. and Kumar, Anil}
}
