Acyloxyetherifications mediated by lead tetracarboxylates
Lead(IV) tetracarboxylates are capable of reacting with unsaturated alcohols to give the products of cyclic acyloxyetherification, usually as a mixture of tetrahydro-2H-pyranyl and tetrahydrofuranyl compounds. © 2008 Elsevier Ltd. All rights reserved.
Main Authors: | Cottrell, I, Moloney, M, Smithies, K |
---|---|
Format: | Journal article |
Language: | English |
Published: |
2009
|
Similar Items
-
Acyloxylactonisations mediated by lead tetracarboxylates
by: Cottrell, I, et al.
Published: (2009) -
Novel alkylation, lactonisation and cascade coupling processes mediated by lead tetracarboxylates: the importance of ligands
by: Moloney, M, et al.
Published: (2002) -
Ligand exchange and catalysis in phenylation reactions mediated by lead tetracarboxylates
by: Moloney, M, et al.
Published: (1998) -
Pb-207 NMR chemical shifts of lead tetracarboxylates
by: Buston, J, et al.
Published: (2001) -
The influence of ligands in Pinhey phenylation reactions using lead(IV) tetracarboxylates
by: Moloney, M, et al.
Published: (1997)