@article { ISI:000283834100025,
	title = {Organocatalytic route to the synthesis of lactone moiety of compactin and mevinolin},
	journal = {Tetrahedron Letters},
	volume = {51},
	number = {44},
	year = {2010},
	month = {NOV},
	pages = {5838-5839},
	publisher = {PERGAMON-ELSEVIER SCIENCE LTD},
	address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND},
	abstract = {<p>An efficient synthesis of lactone moiety of compactin has been achieved. The stereogenic centers were generated by means of iterative proline-catalyzed sequential alpha-aminoxylation and Horner-Wadsworth-Emmons (HWE) olefination of aldehydes. (C) 2010 Elsevier Ltd. All rights reserved.</p>},
	keywords = {Aminoxylation, Compactin, Lactone, organocatalysis, Proline},
	issn = {0040-4039},
	doi = {10.1016/j.tetlet.2010.08.093},
	author = {Kumar, Pradeep and Pandey, Menaka and Gupta, Priti and Dhavale, Dilip D.}
}
@article { ISI:000376689000006,
	title = {Concise enantioselective synthesis of (+)-L-733,060 and (+)-T-2328 via sequential proline catalysis},
	journal = {Synlett},
	volume = {27},
	number = {9},
	year = {2016},
	month = {JUN},
	pages = {1339-1343},
	publisher = {GEORG THIEME VERLAG KG},
	address = {RUDIGERSTR 14, D-70469 STUTTGART, GERMANY},
	abstract = {<p>A new, sequential proline-catalyzed approach to the synthesis of (+)-L-733,060 and (+)-T-2328 in high optical purity (93\% ee) is described starting from phenyl N-Boc imine. The strategy involves proline-catalyzed Mannich reaction of an arylimine with acetaldehyde followed by -aminoxylation/Wittig olefination in a sequential fashion as the key steps.</p>},
	keywords = {Aminoxylation, imine, Mannich reaction, olefination, sequential},
	issn = {0936-5214},
	doi = {10.1055/s-0035-1561346},
	author = {Lalwani, Komal G. and Sudalai, Arumugam}
}
