@article { ISI:000237420200060,
	title = {Hydrophobic effects are dominant over secondary orbital interactions for a simple Diels-Alder reaction in salt solutions},
	journal = {Organic Letters},
	volume = {8},
	number = {10},
	year = {2006},
	month = {MAY},
	pages = {2199-2202},
	publisher = {AMER CHEMICAL SOC},
	type = {Article},
	address = {1155 16TH ST, NW, WASHINGTON, DC 20036 USA},
	abstract = {<p>The stereoselectivity ratios for a Diels-Alder reaction between cyclopentadiene with methyl trans-crotonate carried out in salt solutions demonstrate the dominance of hydrophobic effects over secondary orbital interactions.</p>},
	issn = {1523-7060},
	doi = {10.1021/ol060741q},
	author = {Sarma, D. and Kumar, Anil}
}
@article { ISI:000237820800035,
	title = {Hydrophobic effects in a simple Diels-Alder reaction in water},
	journal = {Tetrahedron Letters},
	volume = {47},
	number = {23},
	year = {2006},
	month = {JUN},
	pages = {3957-3958},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	type = {Article},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>The endolexo ratio for a simple Diels-Alder reaction carried out in water has been used to argue that hydrophobic effects can dominate the geometries of the transition states. (c) 2006 Elsevier Ltd. All rights reserved.</p>},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2006.03.093},
	author = {Sarma, D. and Pawar, S. S. and Deshpande, Suvarna S. and Kumar, Anil}
}
