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- W2071996166 abstract "X-Ray crystal structure analysis of a p-iodobenzoylamino-derivative has established the stereochemistry of the aci-isomers of the ergot alkaloids of the peptide type. The p-iodobenzoyl derivative crystallises as an ethanol solvate with four units of C24H24O5N3I, C2H5OH in an orthorhombic cell, space group P212121, with dimensions a= 15·48, b= 22·28, c= 7·52 A. Phase determination was based initially on the iodine atom and Fourier and least-squares methods were used for the refinement of atomic parameters. The final value of the discrepancy R over the 2292 independent reflexions is 11·2%. The crystal structure reveals an intramolecular OH–benzene hydrogen bond; the proton–benzene distance is ca. 2·1 A. Both five-membered rings in (VI) adopt the envelope conformation." @default.
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- W2071996166 date "1966-01-01" @default.
- W2071996166 modified "2023-10-18" @default.
- W2071996166 title "Fungal metabolites. Part V. X-Ray determination of the structure and stereochemistry of new isomers of the ergot alkaloids of the peptide type" @default.
- W2071996166 doi "https://doi.org/10.1039/j29660000377" @default.
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