@article { ISI:000229484600033,
	title = {Stereoselective syntheses of (+)-alpha- and (-)-beta-conhydrine from L-aspartic acid},
	journal = {Tetrahedron Letters},
	volume = {46},
	number = {23},
	year = {2005},
	month = {JUN},
	pages = {4091-4093},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	type = {Article},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>An efficient synthesis of (+)-alpha-conhydrine 1 and (-)-beta-conhydrine 2 has been achieved by. diastereo selective alkylation of an amino aldehyde derivative 7 with ethylmagnesium bromide or diethylzinc. (c) 2005 Elsevier Ltd. All rights reserved.</p>},
	keywords = {Alkylation, conhydrine, Grignard reaction, Piperidine alkaloids, stereoselectivity},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2005.04.013},
	author = {Pandey, SK and Kumar, P}
}
@article { ISI:000233089900009,
	title = {Wittig-horner approach for the synthesis of tamoxifen},
	journal = {Synthetic Communications},
	volume = {35},
	number = {21},
	year = {2005},
	month = {MAY},
	pages = {2795-2800},
	publisher = {TAYLOR \& FRANCIS INC},
	type = {Article},
	address = {325 CHESTNUT ST, SUITE 800, PHILADELPHIA, PA 19106 USA},
	abstract = {<p>A stereoselective synthesis of Z -tamoxifen, a tetra-substituted alkene with antiestrogenic activity, is described. The Wittig-Horner reaction has been employed as the key step to establish the olefin stereochemistry.</p>},
	keywords = {anticancer drug, phosphonate, stereoselectivity, Tamoxifen, Wittig-Horner reaction},
	issn = {0039-7911},
	doi = {10.1080/00397910500290516},
	author = {Pandey, RK and Wakharkar, RD and Kumar, P}
}
