@article { ISI:000228267300014,
	title = {Simple, concise, stereocontrolled synthesis of (8E,10Z)-pentadecadien-1-ol acetate},
	journal = {Synthetic Communications},
	volume = {35},
	number = {7},
	year = {2005},
	month = {AUG},
	pages = {987-994},
	publisher = {TAYLOR \& FRANCIS INC},
	type = {Article},
	address = {325 CHESTNUT ST, SUITE 800, PHILADELPHIA, PA 19106 USA},
	abstract = {<p>A simple, concise, and stereocontrolled synthesis of (8E, 10Z)-pentadecadien-l -ol acetate involving a Cadiot-Chodkiewicz reaction as the key step is described.</p>},
	keywords = {acetate, Acrobasis vaccini, Cadiot-Chodkiewicz reaction, diacetylene, Pheromone},
	issn = {0039-7911},
	doi = {10.1081/SCC-200051715},
	author = {Chavan, Subhash P. and Kharul, Rajendra K. and Kamat, Subhash K. and Kalkote, Uttam R. and Kale, R. R.}
}
@article { ISI:000356549600021,
	title = {Total synthesis of (+)-petromyroxol},
	journal = {Tetrahedron Letters},
	volume = {56},
	number = {25},
	year = {2015},
	month = {JUN},
	pages = {3933-3935},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>The total synthesis of (+)-petromyroxol establishing its absolute configuration has been accomplished. The strategy developed employs easily accessible carbohydrate building blocks and comprises flexible and scalable chemistry that allowed the synthesis of (+)-petromyroxol along with its three diastereomers varying the stereochemistry mainly at C5 and/or C6. (C) 2015 Elsevier Ltd. All rights reserved.</p>},
	keywords = {Glucose diacetonide, Petromyroxol, Pheromone, Sea Lamprey, Total synthesis},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2015.04.129},
	author = {Mullapudi, Venkanna Babu and Ramana, Chepuri V.}
}
