09-14-2021-0534 - Category: Stereochemistry (locks, clocks and glocks ~ part 1)

Subcategories

This category has the following 6 subcategories, out of 6 total.

C

•  Chirality‎ (3 C, 33 P)

E

•  Enantiopure drugs‎ (110 P)

I

•  Isomerism‎ (2 C, 24 P)

M

•  Molecular geometry‎ (65 P)

R

•  Racemic mixtures‎ (11 P)

S

•  Stereochemists‎ (27 P)

Pages in category "Stereochemistry"

The following 137 pages are in this category, out of 137 total. This list may not reflect recent changes (learn more).

 

• Stereochemistry

A

• Absolute configuration
• Akamptisomer
• Alkane stereochemistry
• Allylic strain
• Anomer
• Antarafacial and suprafacial
• Antipode (chemistry)
• Asymmetric carbon
• Asymmetric induction
• Atropisomer
• Axial chirality

B

• Bailar twist
• Baldwin's rules
• Bent molecular geometry
• Bicapped trigonal prismatic molecular geometry
• Bredt's rule

C

• Cahn–Ingold–Prelog priority rules
• Capped octahedral molecular geometry
• Capped square antiprismatic molecular geometry
• Capped trigonal prismatic molecular geometry
• Chiral analysis
• Chiral auxiliary
• Chiral column chromatography
• Chiral derivatizing agent
• Chiral drugs
• Chiral Lewis acid
• C2-Symmetric ligands
• P-Chiral phosphine
• Chiral resolution
• Chiral switch
• Chirality
• Chirality (chemistry)
• Cis–trans isomerism
• Conformational isomerism
• Coordination number
• Cross-linked enzyme aggregate
• Cryptochirality
• Cryptoregiochemistry
• Cyclohexane conformation

D

• Desymmetrization
• Diastereomer
• Diastereomeric recrystallization
• Diatomic molecule
• Dihedral angle
• Dodecahedral molecular geometry
• Dynamic kinetic resolution in asymmetric synthesis
• Dynamic stereochemistry

E

• E–Z notation
• Eclipsed conformation
• Enantiomer
• Enantiomer self-disproportionation
• Enantiomeric excess
• Enantiopure drug
• Enantioselective synthesis
• Endo-exo isomerism
• Epimer
• Eudysmic ratio

F

• Fischer projection
• Folding (chemistry)
• Fürst-Plattner Rule
• Fuzzy complex

G

• Gauche effect

H

• Haworth projection
• Hexol
• Homochirality
• Homometric structures

I

• Immobilized enzyme
• Inherent chirality

K

• Kinetic resolution
• Klyne–Prelog system
• Kryptoracemic compounds

L

• LCP theory
• Le Bel–Van 't Hoff rule
• Ligand cone angle

M

• Meso compound
• Molecular configuration
• Mosher's acid
• Mutarotation

N

• Natta projection
• Newman projection
• Nitrogen inversion
• Noyori asymmetric hydrogenation

O

• Optical rotation
• Optical rotatory dispersion
• Orbital hybridisation

P

• Pentagonal bipyramidal molecular geometry
• Pentagonal planar molecular geometry
• Pentane interference
• Pfeiffer effect
• Pirkle's alcohol
• Planar chirality
• Prelog strain
• Prochirality
• Proline isomerization in epigenetics
• Protein primary structure
• Protein quaternary structure
• Protein secondary structure
• Pseudorotation
• Pyramidal inversion

R

• Racemic acid
• Racemic mixture
• Racemization
• Ray–Dutt twist
• Regioselectivity
• Residual topology
• Ring flip

S

• Serine octamer cluster
• Soai reaction
• Spontaneous absolute asymmetric synthesis
• Square antiprismatic molecular geometry
• Square planar molecular geometry
• Staggered conformation
• Stereocenter
• Stereochemistry of ketonization of enols and enolates
• Stereoelectronic effect
• Stereoisomerism
• Stereoselectivity
• Stereospecificity
• Steric effects
• Steric number
• Strain (chemistry)
• Supramolecular chirality
• Syn and anti addition

T

• Tacticity
• Thorpe–Ingold effect
• Topicity
• Topoisomer
• Torquoselectivity
• Tricapped trigonal prismatic molecular geometry
• Trigonal bipyramidal molecular geometry
• Trigonal planar molecular geometry
• Trigonal prismatic molecular geometry
• Trigonal pyramidal molecular geometry

V

• Van der Waals strain
• Viedma ripening
• VSEPR theory

https://en.wikipedia.org/wiki/Category:Stereochemistry