TY - JOUR T1 - Asymmetric dihydroxylation route to (R)-(-)-octopamine, (R)-(-)-tembamide and (R)-(-)-aegeline JF - Arkivoc Y1 - 2005 A1 - Sadyandy, R. A1 - Fernandes, R. A. A1 - Kumar, P. KW - aegeline KW - Asymmetric synthesis KW - Dihydroxylation KW - octopamine KW - tembamide AB -

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.

PB - ARKAT USA INC CY - C/O ALAN R KATRITZKY, UNIV FLORIDA, DEPT CHEMISTRY, PO BOX 117200, GAINESVILLE, FL 32611 USA IS - Part 3 U3 -

Foreign

U4 - 1.177 ER -