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Titlebook: Chiral Reactions in Heterogeneous Catalysis; Georges Jannes,Vincent Dubois Book 1995 Springer Science+Business Media New York 1995 Drogen.

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51#
發(fā)表于 2025-3-30 11:38:59 | 只看該作者
José Júlio Alferes,Luís Moniz Pereiramake mechanistic elucidation difficult. In order to alleviate these problems we have been examining the application of novel colloidal catalysts to this reaction. Colloids have been shown to be more active than analogous conventional heterogeneous catalysts because of an increased active metal surfa
52#
發(fā)表于 2025-3-30 13:23:18 | 只看該作者
53#
發(fā)表于 2025-3-30 16:58:47 | 只看該作者
later on became a part ofthe Belgian corporation DCB, still very active in pharmaceuticals today. The school created by Albert Meurice merged in the fifties with another school that had been created to meet the same needs in the field of the food industries, mainly distilleries and breweries. This merger was978-1-4613-5780-3978-1-4615-1909-6
54#
發(fā)表于 2025-3-31 00:43:17 | 只看該作者
An axiomatization of OL and OQLield of chirality..Indeed, while the future development potential offered by chirality is highly promising, several key questions remain to be addressed, such as :.Probably an in-depth objective analysis would yield to a major reassessment of the strategies followed by many players in the field of chirality.
55#
發(fā)表于 2025-3-31 03:16:29 | 只看該作者
56#
發(fā)表于 2025-3-31 08:40:19 | 只看該作者
57#
發(fā)表于 2025-3-31 10:35:10 | 只看該作者
Enzymatic Resolution of Biologically Active Precursors Versus Asymmetric Induction in Heterogeneous ucts like .. Inversion of configuration at C-4 by standard methods should provide the racemic compound ., which easily can be separated from the undesired enantiomer by enzymatic resolution yielding enantiopure . [5] (scheme 1).
58#
發(fā)表于 2025-3-31 16:35:23 | 只看該作者
59#
發(fā)表于 2025-3-31 21:22:17 | 只看該作者
M. Dalla Chiara,R. Giuntini,R. Greechienderstanding of a catalyst‘S enantioselectivity..The most celebrated reaction in enantioselective catalysis with transition metal compounds is the hydrogenation of prochiral olefins, specifically of dehydroamino acids to give amino acids [1]. Scheme 1 shows the hydrogenation of Z-α-acetamido cinnamic acid to N-acetylphenylalanine.
60#
發(fā)表于 2025-3-31 23:21:55 | 只看該作者
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