Stereoselective synthesis of 3-alkylidene/alkylazetidin-2-ones from azetidin-2,3-diones
Title | Stereoselective synthesis of 3-alkylidene/alkylazetidin-2-ones from azetidin-2,3-diones |
Publication Type | Journal Article |
Year of Publication | 2007 |
Authors | Tiwari, DKumar, Shaikh, AY, Pavase, LS, Gumaste, VK, Deshmukh, ARakeeb A |
Journal | Tetrahedron |
Volume | 63 |
Issue | 11 |
Pagination | 2524-2534 |
Date Published | MAR |
Type of Article | Article |
ISSN | 0040-4020 |
Keywords | 3-diones, azetidin-2, azetidin-2-ones, beta-lactam, Grignard reaction |
Abstract | Azetidin-2,3-diones have been used as synthons for the synthesis of C-3 alkylidene/alkylazetidin-2-ones. Some of the 3-alkylazetidin-2-ones are well known for their cholesterol absorption inhibitor activity. A regio and stereoselective Grignard reaction on a keto group followed by dehydration using PPh3/CCl4 reagent is a key step in this synthesis. Hydrogenation of the 3-alkylideneazetidin-2-ones provided stereoselectively cis-3-alkylazetidin-2-ones in very good yields. (c) 2006 Published by Elsevier Ltd. |
DOI | 10.1016/j.tet.2006.12.010 |
Type of Journal (Indian or Foreign) | Foreign |
Impact Factor (IF) | 2.645 |
Divison category:
Organic Chemistry