1379685-76-3Relevant academic research and scientific papers
Enantioselective straightforward access to benzo[b]thiophene analogs of Azatoxin
Gracia, Stéphanie,Marion, Cédric,Rey, Jullien,Popowycz, Florence,Pellet-Rostaing, Stéphane,Lemaire, Marc
, p. 3165 - 3168 (2012)
Horner-Wadsworth Emmons olefination followed by asymmetric hydrogenation allowed the first synthetic access to the chiral thiotryptophan with good enantiomeric excess. Oxazolidinone formation followed by a Pictet-Spengler condensation provided the benzothiophenic analog of Azatoxin.
