Direct NMR evidence of the axial preference of the substituent on phosphorus in 2-chloro- and 2-methoxy-1,2,3-dioxaphosphorinanes.
β Scribed by M. Haemers; R. Ottinger; J. Reisse; D. Zimmermann
- Publisher
- Elsevier Science
- Year
- 1971
- Tongue
- French
- Weight
- 214 KB
- Volume
- 12
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
It was shown by NMR spectmscopy that the 1,3,2-dioxaphosphorinane cycle has a chair conformation [1.2.31. In tricoordinate phosphorus derivatives, the preferred orientation for the substituent on phosphorus (-OR or halogen1 remains a subject of discussion. In fact, proofs of the preferred axiality have been given by different authors [2,4,51 but, until now, results
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