Geometrical isomerism of 4-ethyl-1-methyl-4-phosphorinanol
β Scribed by Louis D. Quin; Howard E. Shook Jr.
- Book ID
- 104223317
- Publisher
- Elsevier Science
- Year
- 1965
- Tongue
- French
- Weight
- 217 KB
- Volume
- 6
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
The configurational stability of the trivalent phosphorus atom is sufficient to permit optically active derivatives to exist (1-J). It follows that suitably substituted cyclic compounds with trivalent phosphorus should exist in cis and trans -isomeric forms.
Qoldwhite (4) has presented evidence from the NMH spectra of substituted 1,3,2-dioxaphospholanes that this may be the case; both the 2-chloro-Q-methyl-and the 2-methoxyh-methyl-derivatives showed the presence of two kinds of C-methyl groups. This effect also was noted for the 2-chlpro-4,4,5,5tetramethyl derivative.
However, the only case of separation
π SIMILAR VOLUMES
We have found that "C nmr spectroscopy is a powerful tool for the determination of the structures of &, trans isomers in the phosphorinane family. It is more definitive than 'H nmr spectroscopy; the carbon signals are well separated and have several unique features pointing to the structure, whereas
In the title compound, C~25~H~23~N~3~O~3~, molecules are linked into chains along the __c__ axis by intermolecular CβH...O hydrogen bonds. The packing is further stabilized by CβH...Ο and ΟβΟ interactions.