01086nas a2200205 4500008004100000245009900041210006900140260011700209300001000326520029100336653001300627653002500640653002000665653001500685653001400700100001700714700002200731700001400753856011300767 2005 eng d00aAsymmetric dihydroxylation route to (R)-(-)-octopamine, (R)-(-)-tembamide and (R)-(-)-aegeline0 aAsymmetric dihydroxylation route to Roctopamine Rtembamide and R aC/O ALAN R KATRITZKY, UNIV FLORIDA, DEPT CHEMISTRY, PO BOX 117200, GAINESVILLE, FL 32611 USAbARKAT USA INCcJAN a36-433 a
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.
10aaegeline10aAsymmetric synthesis10aDihydroxylation10aoctopamine10atembamide1 aSadyandy, R.1 aFernandes, R., A.1 aKumar, P. uhttp://library.ncl.res.in/content/asymmetric-dihydroxylation-route-r-octopamine-r-tembamide-and-r-aegeline-0