stereochemistry's Usage Examples:

An important branch of stereochemistry is the study of chiral molecules.

and nonclassical cannabinoid families, with the 6-hydroxyalkyl chain rigidified with a double bond with defined stereochemistry.

Because palytoxin is such a large molecule, it took some time before the complete structure (including stereochemistry) was elucidated.

their bond connectivity, tautomeric information, isotope information, stereochemistry, and electronic charge information.

In stereochemistry, a torsion angle is defined as a particular example of a dihedral angle.

The alcohol reacts with the phosphine to create a good leaving group then undergoes an inversion of stereochemistry in classic SN2 fashion as the nucleophile displaces it.

Alkane stereochemistry concerns the stereochemistry of alkanes.

The stereochemistry of the natural pheromone was assigned by a combination of synthesis, chiral gas chromatography, and electrophysiological measurement.

See alsoStrain (chemistry)Alkane stereochemistryReferencesChemical bondingPhysical organic chemistry Couture is a commune in the Charente department in southwestern France.

The square planar molecular geometry in chemistry describes the stereochemistry (spatial arrangement of atoms) that is adopted by certain chemical compounds.

In stereochemistry, stereoisomerism, or spatial isomerism, is a form of isomerism in which molecules have the same molecular formula and sequence of bonded.

Palytoxin's stereochemistry was solved first by Moore et al.

In stereochemistry, an epimer is one of a pair of diastereomers.