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Noyori

Noyori "Open" Transition State for non-Chelation Control Aldols... [Pg.82]

Catalytic Asymmetric Synthesis, VCH publishers New York, 1993 (d Noyori, R. Asymmetric Catalysis in Organic Synthesis, Wiley New York, 1994... [Pg.105]

Asymmetric hydrogenation has been achieved with dissolved Wilkinson type catalysts (A. J. Birch, 1976 D. Valentine, Jr., 1978 H.B. Kagan, 1978). The (R)- and (S)-[l,l -binaph-thalene]-2,2 -diylblsCdiphenylphosphine] (= binap ) complexes of ruthenium (A. Miyashita, 1980) and rhodium (A. Miyashita, 1984 R. Noyori, 1987) have been prepared as pure atrop-isomers and used for the stereoselective Noyori hydrogenation of a-(acylamino) acrylic acids and, more significantly, -keto carboxylic esters. In the latter reaction enantiomeric excesses of more than 99% are often achieved (see also M. Nakatsuka, 1990, p. 5586). [Pg.102]

In cases where Noyori s reagent (see p. 102f.) and other enantioselective reducing agents are not successful, (+)- or (—)-chlorodiisopinocampheylborane (Ipc BCl) may help. This reagent reduces prochiral aryl and tert-alkyl ketones with exceptionally high enantiomeric excesses (J. Chandrasekharan, 1985 H.C. Brown, 1986). The initially formed boron moiety is usually removed hy precipitation with diethanolamine. Ipc2BCl has, for example, been applied to synthesize polymer-supported chiral epoxides with 90% e.e. from Merrifield resins (T. Antonsson, 1989). [Pg.108]

In the last fifteen years macrolides have been the major target molecules for complex stereoselective total syntheses. This choice has been made independently by R.B. Woodward and E.J. Corey in Harvard, and has been followed by many famous fellow Americans, e.g., G. Stork, K.C. Nicolaou, S. Masamune, C.H. Heathcock, and S.L. Schreiber, to name only a few. There is also no other class of compounds which is so suitable for retrosynthetic analysis and for the application of modem synthetic reactions, such as Sharpless epoxidation, Noyori hydrogenation, and stereoselective alkylation and aldol reactions. We have chosen a classical synthesis by E.J. Corey and two recent syntheses by A.R. Chamberlin and S.L. Schreiber as examples. [Pg.319]


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Aromatic ketones Noyori

Asymmetric synthesis Noyori reduction

BINAP ligand, Noyori catalytic

BINAP ligands, Noyori catalytic asymmetric

BINAP ligands, Noyori catalytic asymmetric hydrogenation

Bifunctional Noyori

Catalyst Noyori

Diphosphine, Noyori catalytic asymmetric

Enamides Noyori

Enamides, Noyori catalytic asymmetric

Enamides, Noyori catalytic asymmetric hydrogenation

Glycosidation Noyori

Hoffmann-Noyori reaction

Hydrogenation Noyori transfer

Ketones Noyori catalytic asymmetric hydrogenation

Ketones Noyori reduction

NOYORI Chiral Homogeneous Hydrogenation

Noyori Spectroscopy

Noyori annulation

Noyori asymmetric

Noyori asymmetric hydrogenation

Noyori asymmetric reduction

Noyori asymmetric reduction, ketones

Noyori asymmetric transfer

Noyori asymmetric transfer hydrogenation

Noyori catalyst coupling

Noyori catalytic asymmetric hydrogenation mechanism

Noyori cause

Noyori coupling

Noyori defined

Noyori generation

Noyori hydrogenation

Noyori origin

Noyori procedure

Noyori reaction

Noyori reagent

Noyori reduction

Noyori scale

Noyori studies

Noyori techniques

Noyori, Nobel prize

Noyori, Ryoji

Noyori-Ikariya catalyst

Noyori-type catalyst

Noyori-type three-component reaction

Noyori’s

Noyori’s catalyst

Noyori’s reagent

Racemization Noyori catalytic asymmetric hydrogenation

Rhodium complexes Noyori catalytic asymmetric hydrogenation

Ruthenium catalysis Noyori asymmetric hydrogenation

Ruthenium catalysts Noyori-type

Ruthenium complexes, Noyori catalytic

Ruthenium complexes, Noyori catalytic asymmetric hydrogenation

Ruthenium complexes, Noyori catalytic mechanisms

Stereoselective Noyori Reduction

Suzuki, Takamitsu Hosoya, and Ryoji Noyori TECHNOLOGICAL DEVELOPMENTS IN ORGANOPALLADIUM HEMISTRY l Aqueous Palladium Catalysis

Unsaturated alcohols, Noyori catalytic

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