| Title | Construction of protected hydroxylated pyrrolidines using nitrogen-centered radical cyclizations |
| Publication Type | Journal Article |
| Year of Publication | 2009 |
| Authors | Zhai, HM, Zlotorzynska, M, Sammis, G |
| Journal | Chemical Communications |
| Pagination | 5716-5718 |
| Type of Article | Article |
| ISBN Number | 1359-7345 |
| Keywords | 1, 4-DIDEOXY-1, 4-IMINO-L-RIBITOL, ADDITIONS, AMINYL RADICALS, GENERATION, glycosidase, inhibitors, NATURAL OCCURRENCE, ring expansion, ROUTE, STRAIGHTFORWARD SYNTHESIS, THERAPEUTIC APPLICATIONS |
| 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. |
| URL | <Go to ISI>://000270115300013 |
