Niklas, ThomasThomasNiklasSteinmetzger, ChristianChristianSteinmetzgerLiu, WeipingWeipingLiuZell, DanielDanielZellStalke, DietmarDietmarStalkeAckermann, LutzLutzAckermannJohn, MichaelMichaelJohn2018-11-072018-11-072015https://resolver.sub.uni-goettingen.de/purl?gro-2/35787Configurational and conformational characterization of two synthetic -amino acid esters comprising an indan motif was achieved by residual dipolar couplings. We further observed that the stability of Q factors upon addition of structural noise substantially facilitates the selection of the correct structure. The two analyzed compounds differ by a single methyl group, which leads to a remarkable conformational change.journal_article10.1002/ejoc.201500941000363485200002