@article { ISI:000266693600010,
	title = {Formal synthesis of (-) anisomycin via organocatalysis},
	journal = {Arkivoc},
	year = {2009},
	month = {JAN},
	pages = {88-94},
	publisher = {ARKAT USA INC},
	address = {C/O ALAN R KATRITZKY, UNIV FLORIDA, DEPT CHEMISTRY, PO BOX 117200, GAINESVILLE, FL 32611 USA},
	abstract = {<p>An efficient formal synthesis of (-) anisomycin (1), a potent antibiotic agent, has been achieved in good yields and excellent diastereoselectivity. The key steps are proline-catalyzed sequential alpha-amination or alpha-aminoxylation of aldehyde 2 followed by tandem Horner-Wadsworth-Emmons olefination.</p>},
	keywords = {alpha-Amination, alpha-aminoxylation, anisomycin, olefination, Proline},
	issn = {1424-6376},
	author = {Chouthaiwale, Pandurang V. and Kotkar, Shriram P. and Sudalai, Arumugam}
}
@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}
}
