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- W2410027613 abstract "Two dimers (I and II) having 3,3'-disubstituted 2-(2'-indolil)-indoline skeleton were prepared by trifluoroacaetic acid treatment of N-acetyl-L-tryptophan methyl ester. Their CD spectra suggest enantiomeric configuration in 2- and 3-positions of indoline ring. The (-)-enantiomer of skatole dimer has nearly the same CD spectrum as the dimer I. X-ray crystal structure determination of (-)-skatole dimer shows, that it has 2S,3S-trans configuration in the indoline ring suggesting the same configuration of dimer I and opposite, 2R,3R-trans configuration of dimer II." @default.
- W2410027613 created "2016-06-24" @default.
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- W2410027613 date "1999-01-01" @default.
- W2410027613 modified "2023-09-23" @default.
- W2410027613 title "[Stereochemistry of proton catalyzed dimerization of 3-alkyl-indoles]." @default.
- W2410027613 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/10513408" @default.
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