A new route to aristocularine alkaloids: total synthesis of aristoyagonine.
J Org Chem
; 69(13): 4527-30, 2004 Jun 25.
Article
in En
| MEDLINE
| ID: mdl-15202913
ABSTRACT
A short and efficient synthesis of aristocularines, involving the sequential construction of phosphorylated 4-alkoxyisoindolinones, Horner-type reaction, and ultimate cyclization by diaryl ether coupling, is disclosed. The success of this new conceptual approach is demonstrated by the total synthesis of the aristocularine alkaloid aristoyagonine.
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Collection:
01-internacional
Database:
MEDLINE
Main subject:
Fumariaceae
/
Isoquinolines
Language:
En
Journal:
J Org Chem
Year:
2004
Document type:
Article
Affiliation country:
France