Last edited by Doll
Monday, May 11, 2020 | History

2 edition of 2-Siloxetanes: formation, structure and thermal rearrangements. found in the catalog.

2-Siloxetanes: formation, structure and thermal rearrangements.

Wayne Joseph Chatterton

2-Siloxetanes: formation, structure and thermal rearrangements.

by Wayne Joseph Chatterton

  • 342 Want to read
  • 23 Currently reading

Published .
Written in English


The Physical Object
Pagination123 leaves
Number of Pages123
ID Numbers
Open LibraryOL18022377M


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2-Siloxetanes: formation, structure and thermal rearrangements by Wayne Joseph Chatterton Download PDF EPUB FB2

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.

subject area of (Cyclopentadienyl)ruthenium complexes of 3-methoxyestrone. A high-field NMR and x-ray crystallographic study Academic Article ; I-Tetrazines and Inverse-Electron-Demand Diels–Alder Chemistry: A Convenient Radioiodination Strategy for Biomolecule Labeling, Screening, and Biodistribution Studies Academic Article ; 2,5-Bis(diphenylmethylene)cyclopentenone: a solvent.