@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}
}
@article {46352,
	title = {Proline catalyzed sequential alpha-amination/ Prins/ Ritter amidation of aldehydes: new method of construction of tetrahydropyran units},
	journal = {Indian Journal of Chemistry Section B-Organic Chemistry Including Medicinal Chemistry},
	volume = {58},
	year = {2019},
	month = {SEP},
	pages = {1019-1028},
	type = {Article},
	abstract = {<p>An efficient {\textquoteleft}{\textquoteleft}one-pot{\textquoteright}{\textquoteright} synthetic method toward highly substituted tetrahydrofuran (THP) units is reported. The key transformation involves an atom-efficient sequential proline catalyzed alpha-amination of aldehydes to give alpha-aminated aldehydes in situ and the subsequent cyclomerization with homoallylic alcohols under Prins/Ritter conditions. Notably, this method provides access to enantiopure 1,2-syn and 1,4-anti diamino alcohols via reductive ring opening of THP units.</p>
},
	keywords = {alpha-aminoxylation, organocatalysis, Proline catalyzed, sequential, tetrahydropyran unit},
	issn = {0376-4699},
	author = {Ahuja, Brijbhushan and Gadakh, Sunita and Sudalai, Arumugam}
}
