@article { ISI:000288848900007,
	title = {Enantiospecific route to (+)-(1R, 3S)-cis-chrysanthemic acid from (-)-D-pantolactone(1)},
	journal = {Synthesis-Stuttgart},
	number = {7},
	year = {2011},
	month = {APR},
	pages = {1067-1070},
	publisher = {GEORG THIEME VERLAG KG},
	address = {RUDIGERSTR 14, D-70469 STUTTGART, GERMANY},
	abstract = {<p>In this paper, a novel route for the synthesis of (+)-(1R,3S)-cis-chrysanthemic acid is described. The use of readily available (-)-D-pantolactone as a starting point, application of ring-closing metathesis to form the cyclopentene intermediate, and Haller-Bauer/Grob-type fragmentation to form the target compound are the highlights of the present synthesis.</p>},
	keywords = {alkenes, Metathesis, ring closure, stereoselective synthesis, Wittig reaction},
	issn = {0039-7881},
	doi = {10.1055/s-0030-1258451},
	author = {Hajare, Atul K. and Datrange, Laxmikant S. and Murthy, Y. L. N. and Bhuniya, Debnath and Reddy, D. Srinivasa}
}
@article { ISI:000321490900014,
	title = {Synthesis of a sex pheromone of the longtailed mealybug, pseudococcus longispinus},
	journal = {Synthesis-Stuttgart},
	volume = {45},
	number = {12},
	year = {2013},
	month = {JUN},
	pages = {1689-1692},
	publisher = {GEORG THIEME VERLAG KG},
	address = {RUDIGERSTR 14, D-70469 STUTTGART, GERMANY},
	abstract = {<p>The synthesis of a recently identified and highly active sex pheromone of the longtailed mealybug, Pseudococcus longispinus is reported. A concise synthetic route, use of the under explored Meyer-Schuster rearrangement, Claisen rearrangement, and ring-closing metathesis are the highlights of this work.</p>},
	keywords = {Acylation, Metathesis, pheromones, rearrangement, Total synthesis},
	issn = {0039-7881},
	doi = {10.1055/s-0033-1338450},
	author = {Kurhade, Suresh E. and Siddaiah, V. and Bhuniya, Debnath and Reddy, D. Srinivasa}
}
