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Synthesis and 1H, 13C and 31P NMR studies of 2,10-dichloro-6-aryloxy-12H-dibenzo [d,g] [1,3,2]-dioxaphosphocin 6-oxides

✍ Scribed by C. Devendranath Reddy; R. S. N. Reddy; C. Naga Raju; Marwan ElMasri; K. Darrell Berlin; Shankar Subramanian


Publisher
John Wiley and Sons
Year
1991
Tongue
English
Weight
499 KB
Volume
29
Category
Article
ISSN
0749-1581

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✦ Synopsis


Abstract

The spectral analyses and syntheses of several novel 2,10‐dichloro‐6‐aryloxy/alkyl‐12__H__‐dibenzo [d,g] [1,3,2] dioxaphosphocin 6‐oxides have been achieved. Long‐range coupling [^5^J(H,P) = 2.4 Hz] was observed between phosphorus and the bridged methylene protons. Based upon NMR data, a tub‐like conformation is proposed for the central eight‐membered dioxaphosphocin ring. Long‐range ^2^J(P,O,C) and ^3^J(P,O,C,C) couplins were determined, as were the ^31^P chemical shifts for sixteen members of these new heterocycles. A variable‐temperature study of one member suggested the presence of a tub form as a reasonable candidate for one major conformer but the presence of other forms was also implied.


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