Steric hindrance in the synthesis and properties of the dimer of 1-(2,4,6-Tri-tert-butylphenyl)phosphole 1-oxide
✍ Scribed by György Keglevich*; László Toke; Zsolt Böcskei; Veronika Harmat
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 210 KB
- Volume
- 8
- Category
- Article
- ISSN
- 1042-7163
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✦ Synopsis
Steric hindrance was observed during the oxidation of 2,4,6-tri-tert-butylphenylphosphole to the P oxide and in the dimerization of this latter species to the corresponding phosphanorbornene derivative. Single-crystal X-ray analysis of the dimer revealed considerable steric crowding around the P atoms. Deoxygenation of the dimer of the phosphole oxide by Cl 3 SiH-C 6 H 5 N could only be accomplished under forcing conditions at 110ЊC.
📜 SIMILAR VOLUMES
A small variation in the vanadium reagent leads to a completely different product: The cyclooligomerization of phosphaalkynes 2 with tBuN=VCl ⋅DME (DME=1,2-dimethoxyethane) proceeds with incorporation of the imido fragment to give the azatetraphosphaquadricyclanes 1. In contrast, with the correspond