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Kaganer

Murray C B, Kagan C R and Bawendi M G 1995 Self-organization of CdSe nanoorystallites into three-dimensional quantum dot superlattioes Science 270 1335... [Pg.2918]

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]

Another possibility for asymmetric reduction is the use of chiral complex hydrides derived from LiAlH. and chiral alcohols, e.g. N-methylephedrine (I. Jacquet, 1974), or 1,4-bis(dimethylamino)butanediol (D. Seebach, 1974). But stereoselectivities are mostly below 50%. At the present time attempts to form chiral alcohols from ketones are less successful than the asymmetric reduction of C = C double bonds via hydroboration or hydrogenation with Wilkinson type catalysts (G. Zweifel, 1963 H.B. Kagan, 1978 see p. 102f.). [Pg.107]

HORNER - KNOWLES - KAGAN Asymmetric Hydrogenation Enantnselective hydrogenation of prochirai olefins with chiral Rh catalysts... [Pg.180]

Cenum mediated or samarium mediated alkylation ol ketones and aldehydes in the presence of esters see also Kagan-Molander. [Pg.184]

KAGAN-MOLANDER Samanum reagent Lanthanide reagents, speoflcally samanum, lor generation of free radicals useful in cyclizations, reductions... [Pg.196]

This reasoning was set forth by Johnston and Rapp [1961] and developed by Ovchinnikova [1979], Miller [1975b], Truhlar and Kupperman [1971], Babamov and Marcus [1981], and Babamov et al. [1983] for reactions of hydrogen transfer in the gas phase. A similar model was put forth in order to explain the transfer of light impurities in metals [Flynn and Stoneham 1970 Kagan and Klinger 1974]. Simple analytical expressions were found for an illustrative model [Benderskii et al. 1980] in which the A-B and B-C bonds were assumed to be represented by parabolic terms. [Pg.33]

For a review of chemical methods for ilctcimining absolute configuration, see Stereochemistry, Fundamentals and Methods, Vol. 3, H. B. Kagan, ed., G. Thieme, Stuttgart, 1977. [Pg.82]

J. Kagan, Organic Photochemistry, Principles and Applications, Academic Press, San Diego, 1993. [Pg.781]


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See also in sourсe #XX -- [ Pg.2 ]




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Arylethanals Kagan’s ether) from

Asymmetric Synthesis, New Approaches in (Kagan and Fiaud)

Catalyst Kagan

Dubinen-Kaganer equation

Ethers Kagan

General Aspects of Asymmetric Catalysis 1 Non-Linear Effects and Autocatalysis Henri B. Kagan, T. O. Luukas

Historical Perspective Henri B. Kagan

KAGAN MOLANDER Samanum reagent

KAGAN-HORNER-KNOWLES Asymmetric

KAGAN-HORNER-KNOWLES Asymmetric Hydrogenation

KAGAN-MODENA Asymmetric Oxidation

KAGAN-MOLANDER Samarium Reagent

Kagan

Kagan asymmetric sulfur

Kagan asymmetric sulfur oxidation

Kagan oxidation

Kagan procedure

Kagan reagent

Kagan studies

Kagan, Isabelle

Kagan, Jacques

Kagan-Modena-procedure

Kagan-Molander Samarium Diiodide-Mediated Coupling

Kagan-Molander samarium

Kagan-Molander samarium coupling

Kagan-Molander samarium diiodide-mediated

Kagan’s ether

Kagan’s method

Modified Kagan method

Sharpless/Kagan system

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