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Efficient rhodium and iridium-catalysed asymmetric transfer hydrogenation using water-soluble aminosulfonamide ligands

✍ Scribed by Tim Thorpe; John Blacker; Stephen M Brown; Christian Bubert; John Crosby; Steven Fitzjohn; James P Muxworthy; Jonathan M.J Williams


Book ID
104230690
Publisher
Elsevier Science
Year
2001
Tongue
French
Weight
62 KB
Volume
42
Category
Article
ISSN
0040-4039

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✦ Synopsis


A range of aromatic ketones was reduced asymmetrically under transfer hydrogenation conditions using enantiomerically pure catalysts derived from water-soluble diamine ligands and [Cp*MCl 2 ] 2 (Cp*=pentamethylcyclopentadienyl, M=Rh, Ir). High catalytic activity and enantioselectivity were observed in systems containing up to 51% water.


πŸ“œ SIMILAR VOLUMES


Synthesis of water-soluble aminosulfonam
✍ Christian Bubert; John Blacker; Stephen M Brown; John Crosby; Steven Fitzjohn; J πŸ“‚ Article πŸ“… 2001 πŸ› Elsevier Science 🌐 French βš– 85 KB

Water-soluble analogues of Noyori's (1S,2S)-N-(p-tolylsulfonyl)-1,2-diphenylethylenediamine and Knochel's (1R,2R)-N-(p-tolylsulfonyl)-1,2-diaminocyclohexane, containing an additional sulfonic acid group, have been synthesised. The ruthenium catalysed reduction of aromatic ketones using enantiomerica

ChemInform Abstract: Synthesis of Water-
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