The behavior of 2-substituted-1,3-diphenylpropane-1,3-tione toward organophosphorus reagents
β Scribed by L. S. Boulos; R. Shabana; Y. M. Shaker
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 196 KB
- Volume
- 11
- Category
- Article
- ISSN
- 1042-7163
No coin nor oath required. For personal study only.
β¦ Synopsis
The reaction of 2-benzylidene-1,3-diphenylpropanetrione (1a) with phosphorus ylides 2ac afforded the new phosphonium ylides 4a-c. Trialkyl phosphites 3a-c react with 1a to give the respective dialkyl phosphonate products 5a-c. On the other hand, the olefinic compounds 6 and 7 were isolated from the reaction of 1b with Wittig reagents 2. Moreover, trialkyl phosphites reacted with 1b to give products 8a-c. Possible reaction mechanisms are considered, and the structural assignments are based on analytical and spectroscopic evidence.
π SIMILAR VOLUMES
The reaction of 2-thioxo-4-thiazolidinone (1a) with phosphorus ylides 2a and 2b afforded compounds 5 and 6. On the other hand, formylmethylenetriphenylphosphorane (2c) reacts with 1a and its N-methyl derivative 1b to give the new complicated phosphonium ylides 7a,b, respectively. Reactions of 1b wit
The Behavior of 2-Thioxo-4-thiazolidinones Toward Organophosphorus Reagents. -The reactions of the title heterocycles (I) with resonance stabilized phosphonium ylides, dialkyl phosphites, and trialkyl phosphites is studied. Whilst the reactions with ylides give rise to C-alkylated products [cf. (III
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v
4-Hydroxycoumarin (1) reacted with Wittig reagents (2) to give 4-benzoylmethylcoumarin (5A) or [3-(4-hydroxycoumarinyl)]carbonylmethylenetriphenylphosphorane (6) depending upon the nature of the phosphorus ylide used. Dialkyl phosphonates (3a,b) and trialkyl phosphites (4a,b) converted 1 into the re
Electron diffraction / Gas-crystal structure comparison / Conformation The molecular structure of 1,3-diphenylpropane-1,2,3-trione (diphenyl triketone) has been determined by gas-phase electron diffraction at 130Β°C nozzle temperature. It has been found that the phenyl rings are nearly coplanar with