Multiple Interactions between Host Cyclodextrin and Guest Compound Assisting Asymmetrically Selective Reduction with NaBH4in Aqueous Media
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/cl/19/8/19_8_1463/_pdf
Reference4 articles.
1. Asymmetric reduction of arylglyoxylic acids via host-guest complex formation with optically active paracyclophanes.
2. Asymmetric reduction of alkyl aryl ketones in the binding domain of bovine serum albumin
3. Selective reduction of cyclic conjugate enones with sodium borohydride in the presence of cyclodextrins
4. Synthesis of monosubstituted cyclohexaamyloses
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1. Cyclodextrins in Asymmetric and Stereospecific Synthesis;Symmetry;2015-09-24
2. Enzyme Mimics: Cyclodextrins;Encyclopedia of Biomedical Polymers and Polymeric Biomaterials;2015-03-26
3. Reactions Mediated by Cyclodextrins;Molecular Encapsulation;2010-07-13
4. New Aspects of Cyclodextrin Chemistry Induced by Outside Type Complex Formation; Asymmetric Reduction of Indol-3-Pyruvic Acid with NaBH4 in Aqueous Solution;Journal of Inclusion Phenomena and Macrocyclic Chemistry;2006-04-07
5. Organic Reactions Mediated by Cyclodextrins;Chemical Reviews;1998-07-30
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