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Josiphos is a family of chiral phosphinesubstituted<br />

ferrocene ligands useful for<br />

various enantioselective reactions,<br />

especially hydrogenations of C=O and<br />

C=N groups. 1-3 Fluka offers an assortment<br />

of Josiphos ligands with different steric<br />

and electronic properties, to best suit<br />

your specific needs.<br />

Chiral ligands for highly enantioselective hydrogenation and related reactions. The palladium-catalyzed<br />

substitution of allylic acetates by carbon nucleophiles proceeds rapidly, giving high enantioselectivity: 3,4<br />

43167 (R)-1-[(1S)-2-(Diphenylphosphino)ferrocenyl]ethyldicyclohexylphosphine 100mg; 500mg<br />

[(R)-(S)-Josiphos] purum, ~97% Mr 594.54 C36H44FeP2 [155806-35-2]<br />

43168 (S)-1-[(1R)-2-(Diphenylphosphino)ferrocenyl]ethyldicyclohexylphosphine 100mg; 500mg<br />

[(S)-(R)-Josiphos] purum, ≥ 97.0% Mr 594.54 C36H44FeP2 [162291-02-3]<br />

Chiral ligands for homogeneous catalysis: 5,6<br />

43164 (R)-1-[(1S)-2-(Diphenylphosphino)ferrocenyl]ethyldi-tert-butylphosphine 100mg; 500mg<br />

purum, ≥ 97.0% (CHN/NMR) Mr 542.46 C32H40FeP2 [155830-69-6]<br />

43166 (S)-1-[(1R)-2-(Diphenylphosphino)ferrocenyl]ethyldi-tert-butylphosphine 100mg; 500mg<br />

purum, ≥ 97.0% (CHN/NMR) Mr 542.46 C32H40FeP2<br />

Chiral ligands for homogeneous catalysis:<br />

36676 (R)-1-[(1S)-2-(Dicyclohexylphosphino)ferrocenyl]ethyldicyclohexylphosphine 100mg; 500mg<br />

purum, amount Fe ~97% Mr 606.63 C36H56FeP2 [167416-28-6]<br />

36677 (S)-1-[(1R)-2-(Dicyclohexylphosphino)ferrocenyl]ethyldicyclohexylphosphine 50mg; 250mg<br />

purum, amount Fe ~97% Mr 606.63 C36H56FeP2 [158923-07-0]<br />

36678 (R)-1-[(1S)-2-(Dicyclohexylphosphino)ferrocenyl]ethyldiphenylphosphine 50mg; 250mg<br />

purum, ≥ 97.0% (CHN/NMR) Mr 594.54 C36H44FeP2 [158923-09-2]<br />

36679 (S)-1-[(1R)-2-(Dicyclohexylphosphino)ferrocenyl]ethyldiphenylphosphine 50mg; 250mg<br />

purum, ≥ 97.0% (CHN/NMR) Mr 594.54 C36H44FeP2 [162291-01-2]<br />

(1) Blaser, A. H. U. J. Organomet. Chem. 2001, 34, 621. (2) Spindler, B F.; Blaser, A. H. U. Adv. Synth. Catal. 2000, 68, 1. (3) Togni, C. A. et al. J. Am. Chem. Soc.<br />

1994, 116, 4062. (4) Bronco, S. et al. Helv. Chim. Acta 1995, 78, 883. (5) Pregosin, P. S. et al. Organometallics 1995, 14, 842. (6) Zanetti, N.C. et al. ibid. 1996,<br />

15, 860.<br />

Our range of products in this rapidly evolving field is continuously<br />

expanding. For more information, please visit our Web site at<br />

www.sigma-aldrich.com/fluka.

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