Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Formation of Species01:31

Formation of Species

45.4K
Speciation describes the formation of one or more new species from one or sometimes multiple original species. The resulting species are discrete from the parent species, and barriers to reproduction will typically exist. There are two primary mechanisms, speciation with and without geographic isolation—allopatric and sympatric speciation, respectively.
45.4K
Solution Formation02:16

Solution Formation

38.1K
There is no one solvent that can dissolve every type of solute. Some substances that readily dissolve in a certain solvent might be insoluble in a different solvent. A simple way to predict which substances dissolve in which solvent is the phrase "like dissolves like". This means that polar substances, such as salt and sugar, dissolve in a polar substance like water. In contrast, non-polar substances are more soluble in non-polar solvents such as carbon tetrachloride.
This selective...
38.1K
Standard Enthalpy of Formation02:37

Standard Enthalpy of Formation

49.5K
Enthalpy changes are typically tabulated for reactions in which both the reactants and products are at the same conditions. A standard state is a commonly accepted set of conditions used as a reference point for the determination of properties under other different conditions. For chemists, the IUPAC standard state refers to materials under a pressure of 1 bar and solutions at 1 M and does not specify a temperature. Many thermochemical tables list values with a standard state of 1 atm. Because...
49.5K
Formation of Complex Ions03:45

Formation of Complex Ions

26.2K
A type of Lewis acid-base chemistry involves the formation of a complex ion (or a coordination complex) comprising a central atom, typically a transition metal cation, surrounded by ions or molecules called ligands. These ligands can be neutral molecules like H2O or NH3, or ions such as CN− or OH−. Often, the ligands act as Lewis bases, donating a pair of electrons to the central atom. These types of Lewis acid-base reactions are examples of a broad subdiscipline called coordination...
26.2K
Microtubule Formation01:23

Microtubule Formation

7.7K
Microtubules are dynamic structures that undergo continuous assembly and disassembly. They originate from specialized multi-protein complexes known as microtubule organizing centers or MTOCs. Within the MTOC, the point of origin of the microtubule is known as the minus end, while the end radiating outward is the plus end. Microtubules serve two primary functions — the organization of spindle complexes to separate sister chromatids during mitotic or meiotic cell division and the formation...
7.7K
Relationship Formation02:12

Relationship Formation

46.3K
What do you think is the single most influential factor in determining with whom you become friends and whom you form romantic relationships? You might be surprised to learn that the answer is simple: the people with whom you have the most contact. This most important factor is proximity. You are more likely to be friends with people you have regular contact with. For example, there are decades of research that shows that you are more likely to become friends with people who live in your dorm,...
46.3K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Control over stereogenic centres beyond tetracoordination.

Chemical science·2026
Same author

Enantiospecific Optical Sensing of Terpenes by an Aggregated Atropisomeric Platinum(II) Complex.

Angewandte Chemie (International ed. in English)·2026
Same author

Stereoselective total synthesis of skew-tetramantane.

Nature chemistry·2026
Same author

Aromatic ring-opening metathesis.

Nature·2024
Same author

Atroposelective Arene-Forming Wittig Reaction by Phosphorus P<sup>III</sup>/P<sup>V</sup>=O Redox Catalysis.

Angewandte Chemie (International ed. in English)·2024
Same author

Atroposelective catalysis.

Nature reviews. Chemistry·2024
Same journal

Direct impure water electrolysis at industrial scale.

Chemical Society reviews·2026
Same journal

Catalytic valorization of polyolefins: from catalysts and processes to reactors.

Chemical Society reviews·2026
Same journal

Designing stable π-radicals.

Chemical Society reviews·2026
Same journal

Antibacterial drug discovery: challenges and preclinical promises from synthetic small molecules.

Chemical Society reviews·2026
Same journal

Selective carbon-carbon bond cleavage involving alkene moieties.

Chemical Society reviews·2026
Same journal

Circularly polarized luminescence: an easy path from molecules to supramolecular systems and beyond.

Chemical Society reviews·2026
See all related articles

Related Experiment Video

Updated: Feb 12, 2026

Understanding Cerebellar Pattern Formation
13:18

Understanding Cerebellar Pattern Formation

Published on: November 1, 2007

5.5K

Stereoselective arene formation.

Achim Link1, Christof Sparr1

  • 1Department of Chemistry, University of Basel, Switzerland. christof.sparr@unibas.ch.

Chemical Society Reviews
|March 23, 2018
PubMed
Summary
This summary is machine-generated.

Stereoselective arene formation enables the creation of diverse chiral aromatic structures, challenging traditional views in organic chemistry. This approach offers precise control over stereochemistry in complex molecules.

More Related Videos

Microtiter Dish Biofilm Formation Assay
03:57

Microtiter Dish Biofilm Formation Assay

Published on: January 30, 2011

115.0K
The Soft Agar Colony Formation Assay
08:01

The Soft Agar Colony Formation Assay

Published on: October 27, 2014

113.9K

Related Experiment Videos

Last Updated: Feb 12, 2026

Understanding Cerebellar Pattern Formation
13:18

Understanding Cerebellar Pattern Formation

Published on: November 1, 2007

5.5K
Microtiter Dish Biofilm Formation Assay
03:57

Microtiter Dish Biofilm Formation Assay

Published on: January 30, 2011

115.0K
The Soft Agar Colony Formation Assay
08:01

The Soft Agar Colony Formation Assay

Published on: October 27, 2014

113.9K

Area of Science:

  • Organic Chemistry
  • Stereochemistry
  • Asymmetric Synthesis

Background:

  • Aromatic hydrocarbons are typically considered achiral due to their planar and symmetric structures.
  • Current methods for aromatic ring assembly are not commonly used for stereoselective synthesis of chiral compounds.

Purpose of the Study:

  • To challenge the conventional view that aromatic compounds lack chirality.
  • To highlight the potential of stereoselective arene formation for synthesizing a wide array of chiral aromatic molecules.

Main Methods:

  • Review of methodologies for stereoselective arene formation.
  • Analysis of the application of these methods across various molecular scaffolds.

Main Results:

  • Stereoselective arene formation provides access to diverse chiral aromatic structures.
  • Methods allow control over stereocenters, helical chirality, restricted rotation axes, planar chirality, and curved polyaromatics.

Conclusions:

  • Stereoselective arene formation is a powerful strategy for constructing complex chiral aromatic systems.
  • This approach offers significant promise for the synthesis of extended, well-defined chiral architectures.