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ChemInform Abstract: Synthesis and Photolysis of Phosphiranes and Diphosphiranes Carrying Sterically Protecting Groups on the Phosphorus Atoms.

โœ 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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โœฆ 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;


๐Ÿ“œ SIMILAR VOLUMES


Synthesis and photolysis of phosphiranes
โœ Kyoko Tsuji; Shigeru Sasaki; Masaaki Yoshifuji ๐Ÿ“‚ Article ๐Ÿ“… 1998 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 204 KB

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