@article { ISI:000231751000005,
	title = {Efficient total synthesis of iso-cladospolide B and cladospolide B},
	journal = {Tetrahedron Letters},
	volume = {46},
	number = {39},
	year = {2005},
	month = {SEP},
	pages = {6625-6627},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	type = {Article},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>An efficient synthesis of iso-cladospolide B and cladospolide B has been achieved using Jacobsen{\textquoteright}s hydrolytic kinetic resolution (HKR), Sharpless asymmetric dihydroxylation and Yamaguchi macrolactonization as the key steps. (c) 2005 Elsevier Ltd. All rights reserved.</p>},
	keywords = {cladospolide B, Hydrolytic kinetic resolution, iso-cladospolide B, sharpless asymmetric dihydroxylation, Yamaguchi macrolactonization},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2005.07.153},
	author = {Pandey, SK and Kumar, P}
}
@article { ISI:000291302900019,
	title = {Organocatalytic enantioselective approach to the synthesis of verbalactone and (R)-massoialactone},
	journal = {Synthesis-Stuttgart},
	number = {12},
	year = {2011},
	month = {JUN},
	pages = {1954-1959},
	publisher = {GEORG THIEME VERLAG KG},
	address = {RUDIGERSTR 14, D-70469 STUTTGART, GERMANY},
	abstract = {<p>The organocatalytic enantioselective synthesis of verbalactone and (R)-massoialactone is described. The requisite stereogenic centers of the target molecules were constructed using L-proline-catalyzed alpha-aminoxylation and Horner-Wadsworth-Emmons (HWE) olefination. Yamaguchi macrolactonization and ring-closing metathesis were employed as key steps in the syntheses.</p>},
	keywords = {alpha-aminoxylation, Horner-Wadsworth-Emmons olefination, L-proline, massoialactone, Ring-closing metathesis, verbalactone, Yamaguchi macrolactonization},
	issn = {0039-7881},
	doi = {10.1055/s-0030-1260051},
	author = {Harbindu, Anand and Kumar, Pradeep}
}
