945915-41-3Relevant academic research and scientific papers
Stereospecific synthesis of (-)-neplanocin F
Ropero, Sergio Rodriguez,Edmont, Dolores,Mathe, Christophe,Perigaud, Christian
, p. 1111 - 1114 (2008/09/17)
The stereospecific synthesis of (-)-neplanocin F was achieved in 15 steps from 2,3-O-isopropylidene-D-1,4-ribonolactone. The synthetic methodology can give an access through appropriate modifications to new series of carbanucleosides. Copyright Taylor & F
First enantioselective synthesis of (-)-neplanocin F
Rodriguez, Sergio,Edmont, Dolorès,Mathé, Christophe,Périgaud, Christian
, p. 7165 - 7171 (2008/02/07)
(-)-Neplanocin F, the natural isomer of a component of the neplanocin family was enantioselectively synthesized starting from d-γ-ribonolactone. The synthetic approach was based on the preparation of a suitable carbocyclic precursor bearing three hydroxyl
