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Stereochemistry

Table of contents

Enantiopure drugs

Isomerism

Racemic mixtures

Stereochemistry stubs

Stereochemists

Absolute configuration

Akamptisomer

Allylic strain

Anomer

Antarafacial and suprafacial

Asymmetric carbon

Asymmetric induction

Atropisomer

Axial chirality

Baldwin's rules

Bredt's rule

C2-Symmetric ligands

Cahn–Ingold–Prelog priority rules

Chiral Lewis acid

Chiral analysis

Chiral auxiliary

Chiral column chromatography

Chiral derivatizing agent

Chiral drugs

Chiral inversion

Chiral resolution

Chiral switch

Chiral thin-layer chromatography

Chirality

Chirality-induced spin selectivity

Chirality (chemistry)

Chirality timeline

Cis–trans isomerism

Conformational isomerism

Cross-linked enzyme aggregate

Cryptochirality

Cryptoregiochemistry

Cyclohexane conformation

Desymmetrization

Diastereomer

Diastereomeric recrystallization

Dynamic kinetic resolution in asymmetric synthesis

Dynamic stereochemistry

Eclipsed conformation

Enantiomer

Enantiomer self-disproportionation

Enantiomeric excess

Enantiopure drug

Enantioselective synthesis

Endo-exo isomerism

Epimer

Eudysmic ratio

E–Z notation

Fischer projection

Fuzzy complex

Fürst-Plattner Rule

Gauche effect

Haworth projection

Hexol

Homochirality

Homometric structures

Immobilized enzyme

Inherent chirality

Kinetic resolution

Klyne–Prelog system

Kryptoracemic compounds

Le Bel–Van 't Hoff rule

Ligand cone angle

Meso compound

Molecular configuration

Mosher's acid

Mutarotation

Natta projection

Newman projection

Noyori asymmetric hydrogenation

Optical rotation

Optical rotatory dispersion

P-Chiral phosphine

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

Racemic acid

Racemic mixture

Racemization

Regioselectivity

Serine octamer cluster

Soai reaction

Specific rotation

Spontaneous absolute asymmetric synthesis

Staggered conformation

Stereocenter

 Ancestors (5)

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Ciro Santilli 34 Updated 2024-11-19 Created 1970-01-01

Molecules that are the same if you just look at "what atom is linked to what atom", they are only different if you consider the relative spacial positions of atoms.

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