stereochemistry's Usage Examples:

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

Alkane stereochemistry Eclipsed conformation Eliel, Ernest L.

picture the three-dimensional arrangement of atoms in a molecule (stereochemistry).

A Newman projection, useful in alkane stereochemistry, visualizes the conformation of a chemical bond from front to back, with the front atom represented.

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

Chirality is an important concept for stereochemistry and biochemistry.

drug Atropisomerism Chirotechnology Diastereomers Dynamic stereochemistry Stereochemistry Stereogenic "enantiomer - definition of enantiomer in English.

Basic terminology of stereochemistry (IUPAC Recommendations 1996).

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

preferred relative stereochemistry.

In this case, either two or more chiral centers are formed at once such that one relative stereochemistry is favored, or.

Under lithium-free conditions, the stereochemistry of the product 5 is due to the kinetically controlled addition of the.

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

The descriptors only describe relative stereochemistry rather than absolute stereochemistry.

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