655240-18-9Relevant academic research and scientific papers
Regiospecific, Enantiospecific Total Synthesis of the 12-Alkoxy- Substituted Indole Alkaloids, (+)-12-Methoxy-Na-methylvellosimine, (+)-12-Methoxyaffinisine, and (-)-Fuchsiaefoline
Zhou, Hao,Liao, Xuebin,Cook, James M.
, p. 249 - 252 (2004)
(Matrix presented) The enantiospecific synthesis of 7-methoxy-D-tryptophan was completed by combination of the Larock heteroannulation process with a Schoellkopf-based chiral auxiliary in good yield. This ester was then employed in the first total synthes
General approach for the synthesis of 12-methoxy-substituted sarpagine indole alkaloids including (-)-12-methoxy-Nb-methylvoachalotine, (+)-12-methoxy-Na-methylvellosimine, (+)-12-methoxyaffinisine, and (-)-fuchsiaefoline
Zhou, Hao,Liao, Xuebin,Yin, Wenyuan,Ma, Jun,Cook, James M.
, p. 251 - 259 (2007/10/03)
The enantiospecific synthesis of 7-methoxy-D-tryptophan ethyl ester was completed by combination of the Larock heteroannulation process with a Schoellkopf-based chiral auxiliary in good yield. This ester was then employed in the first regiospecific, stere
