@article { ISI:000229484600029,
	title = {Carbohydrate-based approach for the total synthesis of strictifolione},
	journal = {Tetrahedron Letters},
	volume = {46},
	number = {23},
	year = {2005},
	month = {JUN},
	pages = {4073-4075},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	type = {Article},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>A chiral pool approach starting with D-glucose, using the Yamaguchi protocol and a Z-selective HWE reaction followed by lactonization, has been applied to execute the total synthesis of strictifolione. (c) 2005 Elsevier Ltd. All rights reserved.</p>},
	keywords = {D-Glucose, double elimination, Horner-Wadsworth-Emmons reaction, lactonization, strictifolione, Yamaguchi protocol},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2005.04.031},
	author = {Ramana, C. V. and Raghupathi, N. and Gurjar, M. K. and Chorghade, Mukund S.}
}
@article { ISI:000344204600027,
	title = {Total synthesis of mangiferaelactone},
	journal = {Tetrahedron Letters},
	volume = {55},
	number = {45},
	year = {2014},
	month = {NOV},
	pages = {6263-6265},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>Herein we document the first total synthesis of mangiferaelactone and thus establish its absolute configuration. The central nonenolide ring was constructed using ring closing metathesis and Yamaguchi esterification. The key alcohol fragment was synthesized by the Bernet-Vasella fragmentation of C-ribofuranoside. (C) 2014 Elsevier Ltd. All rights reserved.</p>},
	keywords = {Bernet-Vasella fragmentation, Nonenolide, Ring closing metathesis, Total synthesis, Yamaguchi protocol},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2014.09.084},
	author = {Vadhadiya, Paresh M. and Ramana, C. V.}
}
