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- W2520828592 abstract "Nuclear magnetic resonance (NMR) studies of acid-induced conformational switching (trans/cis isomerization) of N,N-diarylamides bearing a pyridine moiety indicated that the trans/cis conformational preference of these amides is dependent on the relative π-electron densities of the two N-aromatic parts, and can be controlled by protonation or deprotonation of pyridine." @default.
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- W2520828592 date "2016-10-01" @default.
- W2520828592 modified "2023-09-25" @default.
- W2520828592 title "Acid-controlled switching of conformational preference of N,N-diarylamides bearing pyridine" @default.
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- W2520828592 doi "https://doi.org/10.1016/j.tetlet.2016.09.035" @default.
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