Allylbutyltin halides (CH2CHCH2)SnBu3−nCln (n = 0, 1, 2, 3). Preparation, carbon-13 NMR characterization and allylstannylation ability towards ketones and aldehydes
- 9 September 1980
- journal article
- Published by Elsevier in Journal of Organometallic Chemistry
- Vol. 197 (1), 45-50
- https://doi.org/10.1016/s0022-328x(00)84453-8
Abstract
No abstract availableThis publication has 18 references indexed in Scilit:
- The transfer of the allyl group from allyl-di-alkyl-carbinols to organotin substratesInorganica Chimica Acta, 1978
- Reversible allylstannation of carbonyl compounds; a new route to mixed allyltins via allylcarbinolsJournal of Organometallic Chemistry, 1978
- Allyltin chlorides in chemical synthesis. Insertion reaction of dibutylallyl- and triallyltin chlorides with methyl-i-propyl-ketoneInorganica Chimica Acta, 1977
- 13C NMR studies of organosilanesJournal of Organometallic Chemistry, 1977
- A convenient synthesis of (C1-C18) alkyltin trihalidesJournal of Organometallic Chemistry, 1975
- The reaction of perhalogenoketones with allylic derivatives of silicon and tinJournal of Organometallic Chemistry, 1975
- Organotin chemistry. Part IV. The preparation of compounds of the composition R2Sn(OMe)XJournal of the Chemical Society C: Organic, 1967
- The preparation and properties of a series of olefinic tin compoundsJournal of Organometallic Chemistry, 1964
- A Convenient Method for Utilizing the Allyl Grignard ReagentThe Journal of Organic Chemistry, 1963
- 273. Preparation and properties of allyl phosphines, arsines, and stannanesJournal of the Chemical Society, 1947