@article { ISI:000278128500009,
	title = {Synthesis of optically pure 2,3,4-trisubstituted tetrahydrofurans via a two-step sequential Michael-Evans aldol cyclization strategy: total synthesis of (+)-magnolone},
	journal = {Tetrahedron Letters},
	volume = {51},
	number = {22},
	year = {2010},
	month = {JUN},
	pages = {2975-2978},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>Synthesis of optically pure 2,3,4-trisubstituted tetrahydrofurans is described employing a two-step Michael-Evans aldol cyclization strategy. The approach is successfully applied for the total synthesis of furano lignan natural product (+)-magnolone. (C) 2010 Elsevier Ltd. All rights reserved.</p>},
	keywords = {HWE reaction, Lignans, Magnolone, Michael-Evans aldol reaction, Tetrahydrofuran},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2010.03.111},
	author = {Pandey, Ganesh and Luckorse, Srikanth and Budakoti, Asha and Puranik, Vedavati G.}
}
