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Noyori asymmetric

H.U. Blaser, Tetrahedron Asymmetiy, 2,843 (1991) R. Noyori, Asymmetric Catalysis in Organic Synthesis, Wiley, New York, 1994.. [Pg.62]

R. Noyori, Asymmetric Catalysis in Organic Synthesis. John Wiley Sons, 1994. [Pg.1419]

J.-L Xiao, S. C. A Nefkens, P. G. Jessop, T. Ikariya, R. Noyori, Asymmetric Hydrogenation of a, -Unsaturated Carboxylic Adds in Supercritical Carbon Dioxide , Tetrahedron Lett. 1996,37,2813-2816. [Pg.25]

E. Katayama, T. Yokozawa, T. Ikaeiya, and R. Noyori, Asymmetric hydrogenation of alkenyl, cyclopropyl, and aryl ketones. RuCl2(xylbinap)(l,2-diamine) as a precatalyst exhibiting a wide scope, J. Am. Chem. Soc. 1998, 120, 13529-13530. [Pg.567]

A diastereoselective Mukaiyama aldol lactonization between thiopyridylsilylketene acetals and aldehydes was used to form the /3-lactone ring in the total synthesis of (-)-panclicin D <1997T16471>. Noyori asymmetric hydrogenation was a key step in a total synthesis of panclicins A-E and was used to establish the stereocenter in aldehyde 140, which in turn directed the stereochemistry of subsequent reactions <1998J(P1)1373>. The /3-lactone ring was then formed by a [2+2] cycloaddition reaction of 140 with alkyl(trimethylsilyl)ketenes and a Lewis acid catalyst. [Pg.354]

For reviews of asymmetric catalytic epoxidations, see (a) R.S. Johnson, K.B. Sharpless, in B.M. Trost, I. Flemming (Eds.), Comprehensive Organic Synthesis, Vol. 7, Pergamon Press, New York, 1991 (b) R. Noyori, Asymmetric Catalysis in Organic... [Pg.118]

T. Ohkuma, M. Kitamura, R. Noyori, Asymmetric Hydrogenation, in Catalytic Asymmetric Synthesis (I. Ojima, Ed.), Wiley-VCH, New York, 2nd ed., 2000, 1-110. [Pg.824]

Vol. I-III, Springer, Berlin, 1999 b) H. Brunner, W. Zetdmeier, Handbook of Enantioselective Catalysis with Transition Metal Compounds, Vol. I-II, VCH, Wein-heim, 1993 c) R. Noyori, Asymmetric Catalysis in Organic Synthesis, Wiley, New York, 1994 d) I. Ojima, (Ed.), Catalytic Asymmetric Synthesis, VCH, Weinheim, 1993 e) D. J. Berrisford, C. Bolm,... [Pg.274]

General reference G. Helmchen, R. W. Hoffmann, J. Mulzer, E. Schaumann (eds.), Houben-Weyt Methods of Organic Chemistry, Vol. E 21, Stereoselective Synthesis, Thieme, Stuttgart, 1995. See also R. Noyori, Asymmetric Catalysis in Organic Synthesis, John Wiley, Chichester, 1994 M. Nogradi, Stereoselective Synthesis, VCH, Wein-heim, 1995 R. S. Atkinson, Stereoselective Synthesis. John Wiley, Chichester, 1995 G. Procter, Asymmetric Synthesis, OUP, Oxford, 1996. [Pg.46]


See other pages where Noyori asymmetric is mentioned: [Pg.389]    [Pg.794]    [Pg.210]    [Pg.824]    [Pg.1024]    [Pg.1189]    [Pg.1190]    [Pg.1275]    [Pg.314]    [Pg.430]    [Pg.26]    [Pg.26]    [Pg.35]    [Pg.139]    [Pg.223]    [Pg.209]    [Pg.121]    [Pg.129]    [Pg.42]    [Pg.580]   


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Enamides, Noyori catalytic asymmetric

Enamides, Noyori catalytic asymmetric hydrogenation

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Noyori

Noyori asymmetric hydrogenation

Noyori asymmetric reduction

Noyori asymmetric reduction, ketones

Noyori asymmetric transfer

Noyori asymmetric transfer hydrogenation

Noyori catalytic asymmetric hydrogenation mechanism

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Ruthenium catalysis Noyori asymmetric hydrogenation

Ruthenium complexes, Noyori catalytic asymmetric hydrogenation

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