951396-65-9Relevant academic research and scientific papers
Total synthesis of (+)- and (-)-galanthamine
Kato, Tomoaki,Tanimoto, Hiroki,Yamada, Hisako,Chida, Noritaka
, p. 563 - 597 (2013/09/12)
The stereoselective total synthesis of (+)-galanthamine [(+)-1], an antipode of the natural product, and (-)-galanthamine [(-)-1] starting from D-glucose is described. The cyclohexene unit in (+)-1 was prepared in an optically active form from D-glucose using Ferrier's carbocyclization reaction, and the benzylic quaternary carbon was stereoselectively generated via chirality transfer by Johnson-or Eschenmoser-Claisen rearrangement. The dibenzofuran skeleton was effectively constructed by the bromonium ion-mediated intramolecular dealkylating etherification. After the introduction of a carbon-carbon double bond, the Pictet-Spengler type cyclization, followed by reduction of an amide function afforded (+)-1. Starting from D-glucose, (-)-galanthamine [(-)-1] was also totally synthesized. The Japan Institute of Heterocyclic Chemistry.
Total synthesis of (+)-galanthamine starting from d-glucose
Tanimoto, Hiroki,Kato, Tomoaki,Chida, Noritaka
, p. 6267 - 6270 (2008/02/10)
The stereoselective total synthesis of (+)-galanthamine (+)-1 starting from d-glucose is described. The cyclohexene ring in (+)-1 was prepared in an optically active form from d-glucose using Ferrier's carbocyclization reaction, and the critical quaternar
