Stereospecific pictet-spengler reaction: synthesis of cis (+)-(1S, 12bR)-1-aminoindoloquinolizidine from a pure α-(S)-aminoaldehyde derivative
摘要:
Pictet-Spengler reaction provides cis (+)-1-(S)-aminoindolo[2,3-a]quinolizidine in an enantio- and diastereoselective manner, using an alpha-aminoaldehyde derived from L-glutamic acid.
Stereospecific pictet-spengler reaction: synthesis of cis (+)-(1S, 12bR)-1-aminoindoloquinolizidine from a pure α-(S)-aminoaldehyde derivative
摘要:
Pictet-Spengler reaction provides cis (+)-1-(S)-aminoindolo[2,3-a]quinolizidine in an enantio- and diastereoselective manner, using an alpha-aminoaldehyde derived from L-glutamic acid.
Stereospecific pictet-spengler reaction: synthesis of cis (+)-(1S, 12bR)-1-aminoindoloquinolizidine from a pure α-(S)-aminoaldehyde derivative
作者:Patricia Melnyk、Pierre Ducrot、Claude Thal
DOI:10.1016/s0040-4020(01)96265-9
日期:1993.9
Pictet-Spengler reaction provides cis (+)-1-(S)-aminoindolo[2,3-a]quinolizidine in an enantio- and diastereoselective manner, using an alpha-aminoaldehyde derived from L-glutamic acid.