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

T Thorpe, J Blacker, S M Brown, C Bubert, J Crosby, S Fitzjohn, J P Muxworthy, J M J Williams

Research output: Contribution to journalArticle

111 Citations (Scopus)

Abstract

A range of aromatic ketones was reduced asymmetrically under transfer hydrogenation conditions using enantiomerically pure catalysts derived from water-soluble diamine ligands and [Cp*MCl2](2) (Cp* = pentamethylcyclopentadienyl, M = Rh, Ir). High catalytic activity and enantioselectivity were observed in systems containing up to 51% water. (C) 2001 Elsevier Science Ltd. All rights reserved.
Original languageEnglish
Pages (from-to)4041-4043
Number of pages3
JournalTetrahedron Letters
Volume42
Issue number24
Publication statusPublished - 2001

Fingerprint Dive into the research topics of 'Efficient rhodium and iridium-catalysed asymmetric transfer hydrogenation using water-soluble aminosulfonamide ligands'. Together they form a unique fingerprint.

  • Cite this

    Thorpe, T., Blacker, J., Brown, S. M., Bubert, C., Crosby, J., Fitzjohn, S., Muxworthy, J. P., & Williams, J. M. J. (2001). Efficient rhodium and iridium-catalysed asymmetric transfer hydrogenation using water-soluble aminosulfonamide ligands. Tetrahedron Letters, 42(24), 4041-4043.