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140122 ||| eng |
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|a 9783642668425
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| 100 |
1 |
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|a Bender, M. L.
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| 245 |
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|a Cyclodextrin Chemistry
|h Elektronische Ressource
|c by M. L. Bender, M. Komiyama
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| 250 |
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|a 1st ed. 1978
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| 260 |
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|a Berlin, Heidelberg
|b Springer Berlin Heidelberg
|c 1978, 1978
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| 300 |
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|a X, 96 p
|b online resource
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| 505 |
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|a I. Introduction -- II. Properties -- 1. Source and Nomenclature -- 2. Structure and Physical Properties -- III. Inclusion Complex Formation -- 1. Detection of Complex Formation and Structure of the Complexes -- 2. The Determination of Dissociation Constants of Inclusion Complexes -- 3. Binding Force of the Complexes -- IV. Catalyses by Cyclodextrins Leading to Practical Usages of Cyclodextrins -- V. Covalent Catalyses -- 1. Hydrolyses of Phenyl Esters -- 2. Hydrolyses of Amides -- 3. Hydrolyses of Organophosphates and Carbonates -- VI. Noncovalent Catalyses -- 1. The Microsolvent Effect -- 2. The Conformational Effect -- VII. Asymmetric Catalyses by Cyclodextrins -- 1. Selective Precipitation of d, l Compounds -- 2. Hydrolyses of Esters -- 3. Cleavage of Organophosphates -- 4. Addition and Oxidation Reactions -- VIII. Improvement by Covalent and Noncovalent Modification -- 1. Acceleration of the Deacylation Step -- 2. Better Models of Hydrolytic Enzymes -- 3. Cyclodextrins Containing Metal Ions -- IX. Conclusion -- References -- Author Index
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| 653 |
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|a Chemistry, Organic
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| 653 |
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|a Organic Chemistry
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| 700 |
1 |
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|a Komiyama, M.
|e [author]
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| 041 |
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7 |
|a eng
|2 ISO 639-2
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| 989 |
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|b SBA
|a Springer Book Archives -2004
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| 490 |
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|a Reactivity and Structure: Concepts in Organic Chemistry
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| 028 |
5 |
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|a 10.1007/978-3-642-66842-5
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| 856 |
4 |
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|u https://doi.org/10.1007/978-3-642-66842-5?nosfx=y
|x Verlag
|3 Volltext
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| 082 |
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|a 547
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| 520 |
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|a Chemistry was at one time completely described in terms of collision theo ry, in which one molecule collided with another, sometimes producing reac tion. Then came the realization that enzymes which are highly efficient ca talysts, work by way of prior complexation, often stereospecific, which is then followed by chemical reaction. Thus, systems that exhibit "host-guest" relationships, i.e., that show complexing are being looked at an ever in creasing frequency. The cyclodextrins are the first and probably the most important example of compounds that exhibits complex formation. This is a book about the cyclodextrins. There are of course other compounds that exhibit "host-guest" relationships and thus bind other organic molecules, but so far they have not achieved the importance of the cyclodextrins. By their name it is obvious that cyclodextrins are cyclic compounds. The complexes that they form are therefore cyclic inclusion complexes. Because the complexes are cyclic in nature, complexation can be very strong, as op posed to 1t-complex, electrostatic, or apolar complexes in which complex formation is two-dimensional rather than three-dimensional. Cyclodextrins turn out to be excellent models of enzymes. This is proba bly not fortuitous because they were first sought since it was discovered that the principal binding in the enzyme chymotrypsin was a cyclic inclusion complex. Cyclodextrins can do more than form cyclic inclusion complexes, they can catalyze as well. But catalysis always occurs after complex formation
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