Cyclodextrins in Asymmetric and Stereospecific Synthesis

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Cyclodextrins in Asymmetric and Stereospecific Synthesis

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wetenschappelijk artikel

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наукова стаття, опублікована у вересні 2015

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Cyclodextrins in Asymmetric and Stereospecific Synthesis

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Cyclodextrins in Asymmetric and Stereospecific Synthesis

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Cyclodextrins in Asymmetric and Stereospecific Synthesis

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Cyclodextrins in Asymmetric and Stereospecific Synthesis

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Cyclodextrins in Asymmetric and Stereospecific Synthesis

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Cyclodextrins in Asymmetric and Stereospecific Synthesis

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P1476

Cyclodextrins in Asymmetric and Stereospecific Synthesis

@en

P2093

Fliur Macaev

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P2860

beta-cyclodextrin-immobilized (4S)-phenoxy-(S)-proline as a catalyst for direct asymmetric aldol reactions.

Cyclodextrin derivatives as chiral selectors for direct gas chromatographic separation of enantiomers in the essential oil, aroma and flavour fields.

Enantiomeric separations of drugs using mixtures of charged and neutral cyclodextrins.

Amino alcohol-modified β-cyclodextrin inducing biomimetic asymmetric oxidation of thioanisole in water.

Recent development of cyclodextrin chiral stationary phases and their applications in chromatography.

A cyclodextrin-modified ketoester for stereoselective epoxidation of alkenes.

Flavin-cyclodextrin conjugates as catalysts of enantioselective sulfoxidations with hydrogen peroxide in aqueous media.

Phosphinocyclodextrins as confining units for catalytic metal centres. Applications to carbon-carbon bond forming reactions.

Cyclodextrins containing an acetone bridge. Synthesis and study as epoxidation catalysts.

Highly efficient asymmetric direct stoichiometric aldol reactions on/in water.

P304

1699-1720

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P31

scholarly article

P356

10.3390/SYM7041699

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P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Veaceslav Boldescu

P577

2015-09-24T00:00:00Z

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