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 Experiment Videos

Catalyzed Asymmetric Arylation Reactions.

Carsten Bolm1, Jens P. Hildebrand, Kilian Muñiz

  • 1Institut für Organische Chemie RWTH Aachen Prof.-Pirlet-Strasse 1, 52056 Aachen (Germany).

Angewandte Chemie (International Ed. in English)
|October 10, 2001
PubMed
Summary

Developing catalytic asymmetric aryl transfer reactions is crucial for organic synthesis. This review covers recent advancements and limitations in enantioselective arylation methods for carbon nucleophiles.

Related Concept Videos

You might also read

Related Articles

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

Sort by
Same author

Y(OTf)<sub>3</sub>-Catalyzed Formal (3 + 2) Cycloadditions of Donor-Acceptor Cyclopropanes with KSCN under Mechanochemical Conditions.

Organic letters·2026
Same author

Mechanochemical Dehydrogenative Phenochalcogenazination: A Pronounced Water Effect.

ChemSusChem·2026
Same author

The accuracy of carbon-13 NMR magnetic-shielding tensors calculated using periodic DFT: a case study on the distinction of crystalline serine phases.

Physical chemistry chemical physics : PCCP·2026
Same author

A Mechanochemical Kolbe-Schmitt Reaction: Catechol Carboxylation Provides Building Blocks for Renewable Plasticizers.

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

Sulfondiimidoyl-Containing Hypervalent Iodine(III) Compounds: Synthesis and Reactivity.

The Journal of organic chemistry·2026
Same author

Iron-Catalyzed Synthesis of Primary Sulfinamidines from Sulfenamides.

Organic letters·2025

Area of Science:

  • Organic Chemistry
  • Asymmetric Catalysis
  • Synthetic Methodology

Background:

  • Carbon nucleophile addition and substitution reactions are foundational in organic synthesis.
  • Catalytic asymmetric variants, particularly enantioselective arylations, lag behind alkylations in maturity and scope.
  • Existing asymmetric arylation protocols often lack general applicability or exhibit limited selectivity.

Purpose of the Study:

  • To review established and emerging methods for catalytic asymmetric aryl transfer.
  • To discuss the scope and limitations of current enantioselective arylation strategies.
  • To highlight recent developments in the field of asymmetric arylation.

Main Methods:

  • Literature review of catalytic asymmetric aryl transfer reactions.

Related Experiment Videos

  • Analysis of established protocols and recent advancements.
  • Discussion of reaction scope, limitations, and selectivity.
  • Main Results:

    • Summarizes key established routes for catalytic asymmetric aryl transfer.
    • Highlights the latest developments and innovations in enantioselective arylation.
    • Identifies limitations in current methodologies, including scope and selectivity issues.

    Conclusions:

    • Catalytic asymmetric aryl transfer remains a challenging but rapidly developing area of organic synthesis.
    • Further research is needed to overcome limitations in generality and selectivity for broader applications.
    • This review provides a comprehensive overview of the current state and future directions in asymmetric arylation.