@article { ISI:000283697400019,
	title = {Stereocontrolled route to the synthesis of (+/-)-3-amino-2,2-dimethyl-1,3-diphenylpropan-1-ol},
	journal = {Tetrahedron Letters},
	volume = {51},
	number = {45},
	year = {2010},
	month = {NOV},
	pages = {5927-5929},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>Both the diastereomers of (+/-)-3-amino-2,2-dimethyl-1,3-diphenylpropan-1-ol were synthesized starting from a common intermediate, namely,B-hydroxy, oxime 6. Diastereoselective reduction with NaBH(4)/TiCl(4) and H(2)-Pd/C provided syn- and anti-isomers, respectively. Good overall yield and selectivity were realized using a simple protocol. (C) 2010 Elsevier Ltd. All rights reserved.</p>},
	keywords = {1, 3-Aminoalcohol, Aldol-Tishchenko reaction, beta-Hydroxy oxime, Diastereoslective reduction},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2010.09.011},
	author = {Patil, M. N. and Bhowmick, Kartick C. and Joshi, Navalkishore N.}
}
