Enantiomers

These enantiomers are mirror images of each other.

The enantiomers of a molecule can have very different biological activities and therapeutic effects.

The two enantiomers of a molecule are non-superimposable mirror images of each other.

Enantiomers are used in chiral synthesis to selectively produce a single product.

The pharmaceutical company is researching the properties of enantiomers to develop drugs with fewer side effects.

The enantiomers of a molecule have identical physical and chemical properties.

There are two types of enantiomers: D and L enantiomers.

The two enantiomers of the compound have identical chemical and physical properties except for their effect on polarized light.

Enantiomers are important in the field of asymmetric synthesis.

The chemist separated the enantiomers to identify the active ingredient in the sample.

The enantiomers of a molecule have the same molecular formula but differ in their spatial arrangement of atoms.

The stereochemistry of enantiomers is important in the field of organic chemistry.

Some natural products exist as enantiomers, such as the amino acid alanine.

Enantiomers have the same molecular formula but differ in the way they are arranged in space.

Enantiomers have different biological activities in the body.

Enantiomers rotate plane-polarized light in opposite directions.

Enantiomers have the same physical and chemical properties except for their optical activity.

The separation of enantiomers is an important step in the production of pharmaceuticals.

Some enantiomers have different smells, such as the "lemon" and "orange" scents of limonene.

The enantiomers of a chiral compound have the same chemical formula but different structures.

The drug must be separated into its enantiomers to determine their biological activity.

The pharmacological activity of a drug can be influenced by its enantiomers.

Enantiomers can be identified by their characteristic circular dichroism spectra.

The study of enantiomers is crucial for understanding the stereochemistry of molecules.

Enantiomers can have different physiological effects in the body, making it important to understand their properties.

Enantiomers of some molecules, such as amino acids, play an important role in biology.

The enantiomers of a compound may have different therapeutic effects.

The study of enantiomers is important in understanding the molecular basis of life.

Enantiomers have the same physical properties but different biological activity.

The synthesis of enantiomers is an important area of research in organic chemistry.

Enantiomers can have different effects on the flavor and aroma of food and beverages.

The different enantiomers of a molecule can have different interactions with other chiral molecules, such as enzymes.

Some enantiomers can have different smells, such as the floral and minty scents of limonene enantiomers.

The presence of enantiomers in a molecule can affect its biological activity and drug metabolism.

Enantiomers can be separated using various analytical techniques, such as chiral chromatography.

Enantiomers can have different physical properties, such as melting and boiling points.

Certain flavors, such as spearmint and caraway, are composed of mixtures of enantiomers.

Many natural compounds, such as amino acids, exist as enantiomers.

The synthesis of enantiomers requires the use of chiral reagents.

The taste of enantiomers can differ significantly.

The resolution of enantiomers using chromatographic methods can be challenging due to their structural similarity.

The characterization of enantiomers using X-ray crystallography can provide valuable information about their three-dimensional structures.

The enantioselective synthesis of natural products often involves the manipulation of enantiomers.

The researchers analyzed the enantiomers present in the sample.

Enantiomers are used in perfumery to create different fragrances.

The study of enantiomers has led to the development of new analytical techniques.

The stereospecificity of enzymatic reactions can lead to the formation of enantiomers.

Enantiomers can have different pharmacokinetic and pharmacodynamic properties.

The chemist explained the properties of enantiomers to his students.

The lab technician separated the enantiomers using a chiral column.