2 edition of 2-Siloxetanes: formation, structure and thermal rearrangements. found in the catalog.
2-Siloxetanes: formation, structure and thermal rearrangements.
Wayne Joseph Chatterton
Published
1987
.
Written in English
| The Physical Object | |
|---|---|
| Pagination | 123 leaves |
| Number of Pages | 123 |
| ID Numbers | |
| Open Library | OL18022377M |
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Intramolecular carbon-hydrogen bond activation of benzyl ligands by metalated cyclopentadienyl derivatives of permethylhafnocene. Molecular structure of .etaC5Me5).eta.5.etaC5Me4CH2)HfCH2C6H5 and the mechanism of rearrangement to its hafnabenzocyclobutene tautomer [cyclic] .etaC5Me5)2Hf(o-CH2C6H4) A.
Ray. Bulls; William P. Schaefer. A variety of relatively stable silenes react with representative nonenolizable aldehydes and ketones to yield moderately stable 1,2-siloxetanes, some of which have been isolated as solids. We use cookies to offer you a better experience, personalize content, tailor advertising, provide social media features, and better understand the use of our services.
Thermal and Photochemical [2+2] Cycloreversion of a 1,2-Disilacyclobutane and a 1,2-Digermacyclobutane. Journal of the American Chemical Society.
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