Phosphiranes and diphosphiranes carrying the 2,4,6-tri-t-butylphenyl or 2,6-dimesityl-4methylphenyl group were synthesized to serve as anticipated phosphinidene-precursors, and their photolyses were investigated by means of 31 P and 1 H NMR, and EPR spectroscopy. Photolysis of the diphosphirane poss
ChemInform Abstract: Synthesis and Photolysis of Phosphiranes and Diphosphiranes Carrying Sterically Protecting Groups on the Phosphorus Atoms.
โ Scribed by Kyoko Tsuji; Shigeru Sasaki; Masaaki Yoshifuji
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 32 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0931-7597
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โฆ Synopsis
Synthesis and Photolysis of Phosphiranes and Diphosphiranes Carrying Sterically Protecting Groups on the Phosphorus Atoms.
-Photolysis of phosphiranes and diphosphiranes possessing a tri-tert-butylphenyl group at the P-atoms proceeds selectively to furnish phosphaindane (XI) as the major product (no yields are given). On the other hand, the inertness of the novel 2,6-dimesityl-4-methyl-phenylphosphirane (VII) under analogous photolysis conditions demonstrates that introduction of the 2,6-dimesityl-4methylphenyl group in place of the tri-tert-butylphenyl group dramatically decreases the photoreactivity.
-(TSUJI, KYOKO; SASAKI, SHIGERU;
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