aluablea-hydroxy acids are conveniently synthesized with relevant selectivityenhancement using a sol-gel hydrophobized nanostructured silica matrix doped withthe organocatalyst TEMPO [Silia*Cat*TMTEMPO] and bleach as primary oxidant,coupled with rapid RuO4-mediated olefin dihydroxylation (Figure 6.1).[1,2]The porousstructure of the fully methyl-modified organically modified silicate (ORMOSIL)xerogel dictates the accessibility of the diol molecules to the entrapped catalystlimiting oxidative cleavage and at the same time preventing catalyst deactivation.

Hydroxylation, Epoxidation and Related Reactions

Ciriminna Rosaria;Pagliaro Mario;
2007

Abstract

aluablea-hydroxy acids are conveniently synthesized with relevant selectivityenhancement using a sol-gel hydrophobized nanostructured silica matrix doped withthe organocatalyst TEMPO [Silia*Cat*TMTEMPO] and bleach as primary oxidant,coupled with rapid RuO4-mediated olefin dihydroxylation (Figure 6.1).[1,2]The porousstructure of the fully methyl-modified organically modified silicate (ORMOSIL)xerogel dictates the accessibility of the diol molecules to the entrapped catalystlimiting oxidative cleavage and at the same time preventing catalyst deactivation.
2007
Istituto per lo Studio dei Materiali Nanostrutturati - ISMN
9780470090220
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Asymmetric epoxidation of trans-?-methylstilbene
Hydroxylation, epoxidation and related reactions
Olefin enantioselective epoxidation using phase transfer conditions
Oxazolidinone ketone catalyst in CIS-olefin asymmetric epoxidation
Oxidative cyclization of 2-(2-alkenyl)phenols
Regio-and diastereoselective oxidative cyclization
VO(acac)2/TBHP in regio-and stereoselective epoxidation
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/462369
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