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

Chemo-differentiating ABB' multicomponent reactions. Privileged building blocks.

David Tejedor1, Fernando García-Tellado

  • 1Instituto de Productos Naturales y Agrobiología, CSIC, Astrofísico Francisco Sánchez 3, 38206 La Laguna, Tenerife, Canary Islands, Spain. dtejedor@ipna.csic.es

Chemical Society Reviews
|February 28, 2007
PubMed
Summary
This summary is machine-generated.

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

Cyanoacrylamide derivatives as a novel amoebicidal agents against Acanthamoeba spp.

Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie·2026
Same author

Targeting Trypanosoma cruzi with indoles: mechanistic insights and implications for human health and Chagas disease therapy.

Bioorganic chemistry·2026
Same author

Catalytic Hydrophosphorylation of Propiolates and Three-Component Phosphorylation of Aldehydes.

The Journal of organic chemistry·2026
Same author

Control of Tetrazine Bioorthogonal Reactivity by Rotaxanation.

Angewandte Chemie (International ed. in English)·2025
Same author

Water as a Reactant: DABCO-Catalyzed Hydration of Activated Alkynes for the Synthesis of Divinyl Ethers.

The Journal of organic chemistry·2024
Same author

<i>E</i>-Cyanoacrylamides and 5-Imino Pyrrolones against <i>Trypanosoma cruzi</i>: Activity and Induced Mechanisms of Cell Death.

Tropical medicine and infectious disease·2024

Multicomponent reactions (MCRs) designated as ABB' introduce one molecule of A and two of B into products chemo-differentiatingly. This simplifies synthesis, making component B a privileged building block for diverse molecular construction.

Area of Science:

  • Organic Chemistry
  • Synthetic Chemistry
  • Reaction Engineering

Background:

  • Multicomponent reactions (MCRs) are efficient for synthesizing complex molecules.
  • Traditional MCRs may lack control over component incorporation.
  • The ABB' MCR designation offers a novel approach to chemo-differentiation.

Purpose of the Study:

  • To define and explore ABB' multicomponent reactions.
  • To highlight the role of component B as a privileged building block.
  • To showcase the advantages of chemo-differentiating MCRs in molecular construction.

Main Methods:

  • Defining ABB' MCRs based on chemo-differentiating incorporation of components A and B.
  • Analyzing the benefits of mixing only two reagents.

Related Experiment Videos

  • Reviewing specific classes of compounds acting as component B.
  • Main Results:

    • ABB' MCRs selectively incorporate one A and two B molecules.
    • Chemo-differentiation in ABB' MCRs simplifies synthetic routes.
    • Component B acts as a versatile, privileged building block.

    Conclusions:

    • ABB' MCRs offer enhanced control and efficiency in synthesis.
    • The concept of chemo-differentiating MCRs expands molecular construction possibilities.
    • Ketenes, alkynoates, carbonyls, enol ethers, and enamines are key building blocks for ABB' MCRs.