950919-15-0Relevant articles and documents
Synthesis of an analogue of lavendamycin and of conformationally restricted derivatives by cyclization via a hemiaminal intermediate
Nourry, Arnaud,Legoupy, Stéphanie,Huet, Fran?ois
, p. 6014 - 6018 (2007)
Quinoline 12 was obtained by a Friedl?nder reaction from 2-aminobenzaldehyde and methyl acetoacetate. Reduction, silylation then oxidation provided compound 8a. A Pictet-Spengler reaction between the latter and tryptophan methyl ester yielded compound 14,