Asymmetric dihydroxylation route to (R)-(-)-octopamine, (R)-(-)-tembamide and (R)-(-)-aegeline
Title | Asymmetric dihydroxylation route to (R)-(-)-octopamine, (R)-(-)-tembamide and (R)-(-)-aegeline |
Publication Type | Journal Article |
Year of Publication | 2005 |
Authors | Sadyandy, R, Fernandes, RA, Kumar, P |
Journal | Arkivoc |
Issue | Part 3 |
Pagination | 36-43 |
Date Published | JAN |
Type of Article | Article |
Keywords | aegeline, Asymmetric synthesis, Dihydroxylation, octopamine, tembamide |
Abstract | A simple and efficient asymmetric synthesis of (R)-(-)-octopamine 1, (R)-(-)-tembamide 2 and (R)-(-)-aegeline 3 is described for the first time employing the Sharpless asymmetric dihydroxylation (AD) as the source of chirality. (C) 2004 Elsevier Science Ltd. All rights reserved. |
Type of Journal (Indian or Foreign) | Foreign |
Impact Factor (IF) | 1.177 |
Divison category:
Organic Chemistry