@article { ISI:000304129000011,
	title = {Organocatalytic sequential alpha-amination/corey-chaykovsky reaction of aldehydes: a high yield synthesis of 4-hydroxypyrazolidine derivatives},
	journal = {Organic Letters},
	volume = {14},
	number = {10},
	year = {2012},
	month = {MAY},
	pages = {2468-2471},
	publisher = {AMER CHEMICAL SOC},
	address = {1155 16TH ST, NW, WASHINGTON, DC 20036 USA},
	abstract = {<p>A tandem reaction of in situ generated a-amino aldehydes with dimethyloxosulfonium methylide under Corey-Chaykovsky reaction conditions proceeds efficiently to give 4-hydroxypyrazolidine derivatives in high yields with excellent enantio- and diastereoselectivities. This organocatalytic sequential method provides for the efficient synthesis of anti-1,2-aminoalcohols, structural subunits present in several bioactive molecules as well.</p>},
	issn = {1523-7060},
	doi = {10.1021/ol300739b},
	author = {Kumar, B. Senthil and Venkataramasubramanian, V. and Sudalai, Arumugam}
}
