Investigating direct routes to an advanced intermediate for the synthesis of C-20 diterpene alkaloids


Autoria(s): Williams, C. M.; Mander, L. N.; Bernhardt, P. V.; Willis, A. C.
Data(s)

01/01/2005

Resumo

Rapid access to the ABCE ring system of the C-20 diterpene alkaloids was achieved by silver (I) promoted intramolecular Friedel-Crafts arylation of a functional group specific 5-bromo-3-azabicyclo[3.3.1]nonane derivative. (c) 2005 Elsevier Ltd. All rights reserved.

Identificador

http://espace.library.uq.edu.au/view/UQ:76569

Idioma(s)

eng

Publicador

Pergamon-Elsevier

Palavras-Chave #Diterpene Alkaloids #Silver (i) #Intramolecular Friedel-crafts Arylation #3-azabicyclo[3.3.1]nonane #Aconite Alkaloids #Hetisine-type #Methyllycaconitine #Ring #Rearrangements #Chemistry #Analogs #Enones #Model #Imide #C1 #250301 Organic Chemical Synthesis #670403 Treatments (e.g. chemicals, antibiotics)
Tipo

Journal Article