Asymmetric dihydroxylation route to (R)-(-)-octopamine, (R)-(-)-tembamide and (R)-(-)-aegeline

TitleAsymmetric dihydroxylation route to (R)-(-)-octopamine, (R)-(-)-tembamide and (R)-(-)-aegeline
Publication TypeJournal Article
Year of Publication2005
AuthorsSadyandy, R, Fernandes, RA, Kumar, P
JournalArkivoc
IssuePart 3
Pagination36-43
Date PublishedJAN
Type of ArticleArticle
Keywordsaegeline, 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