Hydroacylation of Alkenes, Alkynes, and Allenes
The addition of an aldehyde across the C. C multiple bond of an alkene, an alkyne, or an allene delivers a synthetically useful ketone-containing product. The most widely used versions of these transformations are promoted by transition metal complexes, with rhodium catalysts dominating. Intramolecu...
Main Author: | Willis, M |
---|---|
Format: | Book section |
Published: |
Elsevier
2014
|
Similar Items
-
Transition metal catalyzed alkene and alkyne hydroacylation.
by: Willis, M
Published: (2010) -
Traceless chelation-controlled rhodium-catalyzed intermolecular alkene and alkyne hydroacylation.
by: Hooper, J, et al.
Published: (2013) -
Chelation-controlled intermolecular alkene and alkyne hydroacylation: the utility of beta-thioacetal aldehydes.
by: Willis, M, et al.
Published: (2005) -
Exploiting carbonyl groups to control intermolecular rhodium-catalyzed alkene and alkyne hydroacylation
by: Coxon, TJ, et al.
Published: (2017) -
Rhodium-catalyzed intermolecular chelation controlled alkene and alkyne hydroacylation: synthetic scope of beta-S-substituted aldehyde substrates.
by: Willis, M, et al.
Published: (2006)