Selectivity in the Oxidation of Limonene by Amphiphilized Metalloporphyrins in Micellar Media
Authors:
- Stefano BorocciSBStefano Borocci
- Federica MarottiFMFederica Marotti
- Giovanna ManciniGMGiovanna Mancini
- Donato MontiDMDonato Monti
- Alessandra PastoriniAPAlessandra Pastorini
- 18 October 2001
- journal article
- Published by American Chemical Society (ACS) in Langmuir
- Vol. 17 (23) , 7198-7203
Abstract
No abstract availableThis publication has 33 references indexed in Scilit:
- Enantioselective synthesis of β-hydroxy esters by Reformatsky reactions in chiral micellesTetrahedron: Asymmetry, 1997
- Surfactant control of the ratio in the bromination of anilines. 3Tetrahedron, 1996
- Porphyrin Synthesis in Surfactant Solution: Multicomponent Assembly in MicellesThe Journal of Organic Chemistry, 1996
- Chiral Lipophilic Ligands. 1. Enantioselective Cleavage of .alpha.-Amino Acid Esters in Metallomicellar AggregatesThe Journal of Organic Chemistry, 1994
- Effect of micelles on cyclization reactions: the use of N-hexadecyl-2-chloropyridinium iodide as an amphiphilic carboxyl-activating agent in lactonization and lactamizationThe Journal of Organic Chemistry, 1994
- Reduction of Ketones by Sodium Borohydride in the Presence of Cationic SurfactantsJournal of Colloid and Interface Science, 1993
- Regioselective oxidation catalysis in synthetic phospholipid vesicles. Membrane-spanning steroidal metalloporphyrinsJournal of the American Chemical Society, 1989
- Membrane-spanning steroidal metalloporphyrins as site-selective catalysts in synthetic vesiclesJournal of the American Chemical Society, 1987
- Extraordinary micellar enantioselectivity coupled to altered aggregate structureJournal of the American Chemical Society, 1985
- Surfactant control of bromination productsTetrahedron Letters, 1984