Related Experiment Video

Updated: May 16, 2026

Preparation and Reactivity of a Triphosphenium Bromide Salt: A Convenient and Stable Source of Phosphorus(I)
08:46

Preparation and Reactivity of a Triphosphenium Bromide Salt: A Convenient and Stable Source of Phosphorus(I)

Published on: November 22, 2016

Preparation of H,(4) PyrrolidineQuin-BAM (PBAM)

Tyler A Davis, Mark C Dobish, Kenneth E Schwieter

    Organic Syntheses; an Annual Publication of Satisfactory Methods for the Preparation of Organic Chemicals
    |November 28, 2012
    PubMed
    Abstract

    No abstract available in PubMed .

    More Related Videos

    Facile Preparation of 4-Substituted Quinazoline Derivatives
    11:51

    Facile Preparation of 4-Substituted Quinazoline Derivatives

    Published on: February 15, 2016

    [(DPEPhos)(bcp)Cu]PF6: A General and Broadly Applicable Copper-Based Photoredox Catalyst
    09:12

    [(DPEPhos)(bcp)Cu]PF6: A General and Broadly Applicable Copper-Based Photoredox Catalyst

    Published on: May 21, 2019

    Related Experiment Videos

    Last Updated: May 16, 2026

    Preparation and Reactivity of a Triphosphenium Bromide Salt: A Convenient and Stable Source of Phosphorus(I)
    08:46

    Preparation and Reactivity of a Triphosphenium Bromide Salt: A Convenient and Stable Source of Phosphorus(I)

    Published on: November 22, 2016

    Facile Preparation of 4-Substituted Quinazoline Derivatives
    11:51

    Facile Preparation of 4-Substituted Quinazoline Derivatives

    Published on: February 15, 2016

    [(DPEPhos)(bcp)Cu]PF6: A General and Broadly Applicable Copper-Based Photoredox Catalyst
    09:12

    [(DPEPhos)(bcp)Cu]PF6: A General and Broadly Applicable Copper-Based Photoredox Catalyst

    Published on: May 21, 2019

    Related Concept Videos

    Preparation of 1° Amines: Gabriel Synthesis01:28

    Preparation of 1° Amines: Gabriel Synthesis

    Direct alkylation is not a suitable method for synthesizing amines because it produces polyalkylated products. Gabriel synthesis is the most preferred method to exclusively make primary amines. The method uses phthalimide, which contains a protected form of nitrogen that participates in alkylation only once to predominantly give primary amines.
    Strong bases like NaOH or KOH deprotonate the phthalimide to form the corresponding anion, which acts as a nucleophile. Further, the anion attacks an...
    α-Bromination of Carboxylic Acids: Hell–Volhard–Zelinski Reaction01:15

    α-Bromination of Carboxylic Acids: Hell–Volhard–Zelinski Reaction

    The method to achieve α-brominated carboxylic acids using a mixture of phosphorus tribromide and bromine is known as the Hell–Volhard–Zelinski reaction. The reaction is catalyzed by phosphorus tribromide, which can be used directly or produced in situ from red phosphorus and bromine. The mechanism comprises PBr3 catalyzed conversion of acid to acid bromide and hydrogen bromide. The acid bromide enolizes to its enol form in the presence of HBr. The nucleophilic enol attacks the bromine molecule...

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

    Recognition of a Conserved Minimal Catalaphile Explains Catalyst Generality in Enantioselective Nitroalkene Reductions.

    ACS catalysis·2026

    Performance-enhancing asymmetric catalysis unlocks tuning without rebuilding.

    Chem catalysis·2026

    Introduction of a single carboxylic acid converts the cyclic oligomeric depsipeptide ent-verticilide from a ryanodine receptor 2 (RyR2) inhibitor to RyR2 activator.

    Molecular pharmacology·2025

    Elucidating Fluorine Steering Effects in Diels-Alder Reactions Interfaced with Charge-Enhanced Reactivity.

    European journal of organic chemistry·2025

    Total Synthesis of Feglymycin Using Umpolung Amide Synthesis.

    Angewandte Chemie (International ed. in English)·2025

    Performance-Enhancing Asymmetric Catalysis Driven by Achiral Counterion Design.

    Journal of the American Chemical Society·2025

    Large-Scale NaBr/Selectfluor Mediated Alcohol Oxidation: Conversion of (-)-Borneol into (-)-Camphor.

    Organic syntheses; an annual publication of satisfactory methods for the preparation of organic chemicals·2025

    CAREPath: semantic context-aware reasoning paths with mechanism-augmented embeddings for drug repurposing.

    Briefings in bioinformatics·2026

    SOLiD-MaP: A Photoproximity Labeling Platform for Small Molecule Binding Site Mapping on RNA.

    Angewandte Chemie (International ed. in English)·2026

    DAPhen vs BLPhen: Transposition of Coordination Centers Redirects the Metal Binding Affinity.

    Inorganic chemistry·2026

    Predictors of suicide attempt versus isolated suicidal ideation in major depressive disorder: Novel insights from LASSO-boruta screening and binary logistic regression.

    Psychiatry research·2026

    The shelved pipeline: AI can find strategically abandoned medicines and bring them to patients.

    Drug discovery today·2026

    Structure-based design of a 1H-Tetrazole-containing scaffold for Caspase-1 inhibition: Synthesis, biological evaluation, and preliminary in Vivo studies.

    Bioorganic & medicinal chemistry·2026
    See all related articles
    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
    Jove
    Visualize
    Contact Us