Syntheses and Synthetic Applications of Stannylated Allylic Alcohols
The Journal of Organic Chemistry2006Vol. 71(6), pp. 2429–2433
Citations Over TimeTop 11% of 2006 papers
Abstract
Allenyl carbinols undergo regioselective hydrostannation in the presence of MoBl3, a catalyst originally developed for the hydrostannation of alkynes, giving rise to allyl stannanes. These allyl stannanes can easily be converted into useful synthetic building blocks such as allyl iodides or vinyl epoxides.
Related Papers
- → Transition metal-catalyzed allylic substitution reactions with unactivated allylic substrates(2015)668 cited
- → Recent Advances in the Regioselective Synthesis of Pyrazoles(2011)73 cited
- → One-Pot Synthesis of Homoallylic Alcohols via a Facile Conversion of Allylic Alcohols into Allylic Iodides(1989)30 cited
- → β-Aminoenones in the regioselective synthesis of 1,3,5-trialkylpyrazoles. The influence of the substituents in the mechanism and the regioselectivity of the reaction(1998)12 cited
- → ChemInform Abstract: Transition Metal‐Catalyzed Allylic Substitution Reactions with Unactivated Allylic Substrates(2015)