@article {2682,
	title = {Construction of protected hydroxylated pyrrolidines using nitrogen-centered radical cyclizations},
	journal = {Chemical Communications},
	number = {38},
	year = {2009},
	note = {ISI Document Delivery No.: 498CXTimes Cited: 3Cited Reference Count: 41Zhai, Huimin Zlotorzynska, Maria Sammis, Glenn},
	pages = {5716-5718},
	type = {Article},
	abstract = {Nitrogen-centered radical cyclizations onto silyl enol ethers were utilized for the syntheses of protected polyhydroxylated pyrrolidines 2-hydroxymethyl-3-hydroxypyrrolidine and 1,4-dideoxy-1,4-imino-L-ribitol.},
	keywords = {1, 4-DIDEOXY-1, 4-IMINO-L-RIBITOL, ADDITIONS, AMINYL RADICALS, GENERATION, glycosidase, inhibitors, NATURAL OCCURRENCE, ring expansion, ROUTE, STRAIGHTFORWARD SYNTHESIS, THERAPEUTIC APPLICATIONS},
	isbn = {1359-7345},
	url = {<Go to ISI>://000270115300013},
	author = {Zhai, H. M. and Zlotorzynska, M. and Sammis, G.}
}
