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Direct NMR evidence of the axial preference of the substituent on phosphorus in 2-chloro- and 2-methoxy-1,2,3-dioxaphosphorinanes.

✍ 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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✦ 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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