505086-79-3Relevant academic research and scientific papers
Synthesis of chiral 2′,3′-pyranone(pyrrolidinone)-fused tryptamines
Dardennes, Emmanuel,Kovács-Kulyassa, árpád,Renzetti, Andrea,Sapi, Janos,Laronze, Jean-Yves
, p. 221 - 223 (2003)
Chiral pyrano- and pyrrolidino-fused tryptamines were prepared by a diasteroselective trimolecular condensation between indole, Garner's aldehyde and Meldrum's acid, followed by selective functional group transformations.
Diastereocontrolled multicomponent pathway to 3,4-heterocycle-annulated tetrahydro-β-carbolines
Dardennes, Emmanuel,Kovacs-Kulyassa, Arpad,Boisbrun, Michel,Petermann, Christian,Laronze, Jean-Yves,Sapi, Janos
, p. 1329 - 1339 (2007/10/03)
A diastereoselective synthesis, using the Yonemitsu-type trimolecular condensation as the key step, has been used for the preparation of 3,4-heterocycle(furanone-, pyrrolidinone- and pyranone-) annulated tetrahydro-β-carbolines. The chirality of D-gly-cer
