Abstract
The most common and hence commercially available cyclodextrins consist of 6, 7, or 8 α-1,4-linked D-glucosyl units, which form a conical bucket-like structure. The remaining hydroxyl groups, that is, 2-OH, 3-OH, and 6-OH, are all placed on the outside of the bucket, making it polar and hydrophilic. The cavity, however, is apolar and can therefore bind small hydrophobic compounds. The ability to complex apolar molecules in their cavity, thereby making them soluble in aqueous solvents, has led to many industrial uses, especially as a food ingredient and as a flavor/aroma stabilizer. In particular, the complexation of compounds in aqueous solutions has gained interest, and cyclodextrin-based artificial enzymes (chemzymes) have been developed during the last three decades.
Original language | English |
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Title of host publication | Organic synthesis and molecular engineering |
Editors | Mogens Brøndsted Nielsen |
Number of pages | 28 |
Publisher | Wiley |
Publication date | 25 Oct 2013 |
Pages | 305-332 |
Chapter | 11 |
ISBN (Print) | 9781118150924 |
ISBN (Electronic) | 9781118736449 |
DOIs | |
Publication status | Published - 25 Oct 2013 |