Synthesis and antimicrobial activity of 3-(N-arylamino)-2-phenyl-naphtho[1,3-d]-1,2-oxaphosphole 2-oxides
✍ Scribed by P. Haranath; U. Anasuyamma; C. Naga Raju; C. Devendranath Reddy; C. Suresh Reddy
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2005
- Tongue
- English
- Weight
- 97 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0022-152X
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✦ Synopsis
Abstract
The efficient preparation of cis‐3‐(N‐arylamino)‐2‐phenylnaphtho[1,3‐d]‐1,2‐oxaphosphole 2‐oxides 4 and 5 is described by a three‐component reaction involving phenyldichlorophosphine (2) 1‐hydroxy‐2‐naph‐thaldehyde/1‐hydroxy‐2‐acetonaphthone (1) and different substituted amines (3) in anhydrous benzene. The stereo structure, of the products (4 and 5), as well as the reaction mechanism of the cyclization is discussed. The title compounds (4 and 5) were fully characterized by NMR and mass spectral data. Their anti microbial activity was evaluated
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## Abstract Several 2‐alkylcarbamato/thiocarbamato/aryloxy/trichloromethyl‐2,3‐dihydro‐5‐propoxy‐1__H__‐1,3,2‐benzodiazaphosphole 2‐oxides (**4** and **6**) were synthesised by reacting 4‐propoxy‐__o__‐phenylenediamine (**1**) with various __N__‐dichlorophosphinyl carbamates (**3**), aryl phosphoro