104420-84-0Relevant articles and documents
Diastereoselective Synthesis of Cularine Alkaloids via Enium Ions and an Easy Entry to Isoquinolines by Aza-Wittig Electrocyclic Ring Closure
Rodrigues, J. Augusto R.,Abramovitch, Rudolph A.,De Sousa, Joana D. F.,Leiva, Genaro C.
, p. 2920 - 2928 (2007/10/03)
In preliminary communications, we reported the diastereoselective synthesis of cularine and sarcocapnine via the intramolecular ring closure of nitrenium and oxenium ions, a new highly diastereoselective reductive methylation with (+)-8-phenylmenthyl chloroacetate followed by reduction with sodium borohydride, and a facile entry to the isoquinoline precursors by aza-Wittig electrocyclic ring closure. We now report the full details of the syntheses of (+)-O-demethylcularine, (+)-cularine, (+)-sarcocapnidine, (+)-sarcocapnine, and (+)-crassifoline and describe different methods of synthesis of their precursors.
DEMETHYLATIONS IN THE CULARINE SERIES
Lera, Angel Rodriquez de,Villaverde, Carmen,Castedo, Luis
, p. 109 - 113 (2007/10/02)
Selective demethylation in 7,4',5'-substituted cularine compounds can be achieved under two different sets of conditions (acidic and nucleophilic).Less satisfactory results are obtained in the 7,3',4'-substituted analogs.
