𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Unusual products in the reactions of hexachlorocyclotriphosphazatriene with sodium aryloxides

✍ Scribed by Adem Kiliç; Saliha Begeç; Bekir Çetinkaya; Tuncer Hökelek; Zeynel Kiliç; Necla Gündüz; Mustafa Yildiz


Publisher
John Wiley and Sons
Year
1996
Tongue
English
Weight
707 KB
Volume
7
Category
Article
ISSN
1042-7163

No coin nor oath required. For personal study only.

✦ Synopsis


Reactions of hexachlorocyclotriphosphazatriene, N,P,CI, 1, with sodium aryloxides have been studied. Compound 1 was found to react by the nucleophilic substitution pathway to yield monocyclophosphazenes [N,P3Cl,4,6) 5 and N3P3CI4(OC6H2 Me-4-Bui-2,6), 61 and bi(cyc1ophosphazenes) Phosphorus-Nitrogen Compounds. Part 3 [ 11. "To whom correspondence should be addressed. molecule in the asymmetric unit.


📜 SIMILAR VOLUMES


Oximes as intermediates or final product
✍ J. Suwińaski; K. Świerczek; P. Wagner; M. Kubicki; T. Borowiak; J. Stowikowska 📂 Article 📅 2003 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 79 KB

## Abstract It has been shown that reactions of 4‐nitroimidazoles and some other nitroaromatic systems with phenyl‐acetonitrile in the presence of sodium methoxide in methanol lead to the reduction of the nitro to nitroso group and to the nucleophilic displacement of hydrogen atom at the ring by th