Abstract
Chirality plays a central role in the world around us, with nature and scientists producing an ever-increasing number of chiral molecules that have a wide range of different applications. The word chirality is used as a term to describe a molecule whose enantiomers are non-superimposable on their mirror images. A chiral molecule that contains a single stereogenic center may exist in an enantiopure form or as a mixture of enantiomers in varying ratios. Enantiomers exhibit identical physical and chemical properties when present in an achiral environment; however, they often behave very differently when placed in a chiral environment. Many biologically active molecules such as proteins, nucleic acids, and sugars are chiral biopolymers that are constructed from homochiral building blocks.
Original language | English |
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Title of host publication | Comprehensive Chirality |
Subtitle of host publication | Volume 8 - Separations and Analysis |
Editors | E. M. Carreira, H. Yamamoto |
Place of Publication | London, U. K. |
Publisher | Elsevier |
Pages | 571-599 |
Number of pages | 29 |
ISBN (Print) | 9780080951683 |
DOIs | |
Publication status | Published - Sept 2012 |
Keywords
- Absolute configuration
- Chiral derivatizing agent
- Diastereomeric ratio
- Enantiomeric excess
- NMR spectroscopic analysis