101376-66-3Relevant academic research and scientific papers
Diazepinoquinolines with L-Amino Acid Moiety - Preparation and Reactions
Bohnert, Sabine,Guendel, Wolf-H.
, p. 1167 - 1173 (2007/10/02)
Quaternary salts of the amides of N-(3-quinolinecarbonyl)-N-alkyl-amino acids (6) cyclise under the influence of base to the title compounds (7).This intramolecular addition is a reaction with high diastereoselectivity, dependent on the amino acid part. 7
Cyclization to Pyrrolodiazepino-quinoline, a Diastereoselective Reaction
Guendel, Wolf-H.,Bohnert, Sabine
, p. 1127 - 1130 (2007/10/02)
Quaternary salts of N-(3-quinolinylcarbonyl)-L-prolinamide 5b,c cyclize under the influence of base to pyrrolodiazepino-quinolines 6b,c with an additional dissymmetric carbon atom.The reaction yields the pure enantiomers 6b,c with high diastereoselectivit
