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Conformations of erythro- and threo-dimethylacetylcholine iodides in the solid state

✍ Scribed by Eli Shefter; Phyllis Sackman; William F. Stephen Jr.; Edward E. Smissman


Publisher
John Wiley and Sons
Year
1970
Tongue
English
Weight
436 KB
Volume
59
Category
Article
ISSN
0022-3549

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## Abstract The solid‐state and solution conformations of (+)‐chelidonine (1), a biologically active alkaloid, were determined by X‐ray diffraction and ^1^H‐NMR spectroscopy, X‐Ray diffraction analysis revealed a conformer with B/C β€˜__anti__‐type’ __cis__ conjunction, a half‐chair of ring B, and a

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## Synopsis Cyclolinopeptide A, a cyclic nonapeptide isolated from linseed, has lately attracted large interest for i t s cytoprotective activity. The recent elucidation of its solid state structure has prompted us to undertake a detailed conformational analysis in solution. Room-temperature 'H-nm