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.
📜 SIMILAR VOLUMES
## Abstract Synthesis of several novel 6‐aryloxy/arylmio/chloroethoxy‐2,10‐dichloro‐4,8‐dinitro‐12‐trichloro‐memyl‐12__H__‐dibenzo[__d,g__][1,3,2]dioxaphosphocin 6‐oxides (**4a‐k**) was accomplished by reacting 2,2‐bis (2‐hydroxy‐5‐chloro‐3‐nitrophenyl)‐1,1,1‐trichloroethane **2** with different ar
Syitliesis of several 6-sicbstittcted-I ,2,4,8,10.1 I -hexachloro-1 ZH-dibeiizo[d,g][l,3,2]dioxaphosphocin 6oxides and their IR. IH, I3C, and 31P N M R aizd inass spectral analyses are described. Observation of geminal coupling ['J(H,H, = 16.0 Hz] between bridged methylene protons ( 1 2-CH2) suggest