General and efficient route to 3 `-deoxy-3 `-N-, S-, and C-substituted altropyranosyl thymines from 2',3'-O-anhydro-mannopyranosylthymine
Title | General and efficient route to 3 `-deoxy-3 `-N-, S-, and C-substituted altropyranosyl thymines from 2',3'-O-anhydro-mannopyranosylthymine |
Publication Type | Journal Article |
Year of Publication | 2007 |
Authors | Deshpande, SG, Pathak, T |
Journal | Tetrahedron |
Volume | 63 |
Issue | 3 |
Pagination | 602-608 |
Date Published | JAN |
Type of Article | Article |
ISSN | 0040-4020 |
Abstract | An efficient route to 1-(2,3-O-anhydro-4,6-O-phenylmethylene–D-mannopyranosyl) thymine from 1,2,4,6-tetra-O-acetyl-3-O-tosyl-beta-D-glucopyranose has been devised. This newly synthesized epoxide is opened up regioselectively at the C-3'-position by N-, S-, and C-nucleophiles to afford a wide range of new 3-deoxy-3'-substituted altropyranosyl thymines. (c) 2006 Published by Elsevier Ltd. |
DOI | 10.1016/j.tet.2006.11.025 |
Type of Journal (Indian or Foreign) | Foreign |
Impact Factor (IF) | 2.645 |
Divison category:
Organic Chemistry