Related Experiment Video

Updated: May 2, 2026

Preparation of N-2-alkoxyvinylsulfonamides from N-tosyl-1,2,3-triazoles and Subsequent Conversion to Substituted Phthalans and Phenethylamines
10:42

Preparation of N-2-alkoxyvinylsulfonamides from N-tosyl-1,2,3-triazoles and Subsequent Conversion to Substituted Phthalans and Phenethylamines

Published on: January 3, 2018

9.4K

Covalently linked plasticizers: triazole analogues of phthalate plasticizers prepared by mild copper-free “click”

Aruna Earla, Rebecca Braslau

    Macromolecular Rapid Communications
    |March 20, 2014
    PubMed

    More Related Videos

    Design, Synthesis, and Photochemical Properties of Clickable Caged Compounds09:44

    Design, Synthesis, and Photochemical Properties of Clickable Caged Compounds

    Published on: October 15, 2019

    14.8K
    Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives09:22

    Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives

    Published on: February 7, 2017

    7.2K

    Related Concept Videos

    Ziegler–Natta Chain-Growth Polymerization: Overview01:17

    Ziegler–Natta Chain-Growth Polymerization: Overview

    Ziegler–Natta polymerization is another form of addition or chain‐growth polymerization used for synthesizing linear polymers over branched polymers. The catalyst used for polymerization is the Ziegler–Natta catalyst, named after Karl Ziegler and Giulio Natta, who developed it in 1953. This catalyst is an organometallic complex of titanium tetrachloride and triethyl aluminum, with the active form of the catalyst being an alkyl titanium compound. Using the Ziegler–Natta...
    2.3K
    Bioplastics01:27

    Bioplastics

    Bioplastics derived from microbial processes present a sustainable alternative to conventional petroleum-based plastics. Among these, polyhydroxyalkanoates (PHAs), particularly polyhydroxybutyrates (PHBs), have emerged as prominent candidates due to their biodegradability and biocompatibility. These polymers are synthesized by a variety of bacteria, such as Cupriavidus necator and Pseudomonas putida, which naturally accumulate PHAs as intracellular carbon and energy reserves, especially under...
    70
    Aryldiazonium Salts to Azo Dyes: Diazo Coupling01:11

    Aryldiazonium Salts to Azo Dyes: Diazo Coupling

    The reaction of weakly electrophilic aryldiazonium (also called arenediazonium) salts with highly activated aromatic compounds leads to the formation of products with an —N=N— link, called an azo linkage. This reaction, presented in Figure 1, is known as diazo coupling and occurs without the loss of the nitrogen atoms of the aryldiazonium salt. Highly activated aromatic compounds such as phenols or arylamines favor the diazo coupling reaction. The coupling generally occurs at the...
    3.2K
    Olefin Metathesis Polymerization: Ring-Opening Metathesis Polymerization (ROMP)01:16

    Olefin Metathesis Polymerization: Ring-Opening Metathesis Polymerization (ROMP)

    Ring-opening metathesis polymerization or ROMP involves strained cycloalkenes as starting materials. The mechanism of ROMP proceeds by reacting cycloalkene with Grubbs catalyst to give metallacyclobutane intermediate which undergoes a ring-opening reaction to form new carbene. The new carbene reacts with another molecule of cycloalkene. Repetition of these steps leads to the formation of an unsaturated open-chain polymer product. All these steps are reversible, however, relieving the ring...
    2.3K
    Electrophilic Addition to Alkynes: Hydrohalogenation02:35

    Electrophilic Addition to Alkynes: Hydrohalogenation

    Electrophilic addition of hydrogen halides, HX (X = Cl, Br or I) to alkenes forms alkyl halides as per Markovnikov's rule, where the hydrogen gets added to the less substituted carbon of the double bond. Hydrohalogenation of alkynes takes place in a similar manner, with the first addition of HX forming a vinyl halide and the second giving a geminal dihalide.
    9.3K
    Phosphodiester Linkages01:01

    Phosphodiester Linkages

    Overview
    Phosphodiester bond forms when a phosphoric acid molecule (H3PO4) links with two hydroxyl groups (–OH) of two other molecules, forming two ester bonds. Two water molecules are released in this process. The phosphodiester bond is commonly found in nucleic acids (DNA and RNA) and plays a critical role in their structure and function.
    Phosphodiester Bonds Link Nucleotides Together
    DNA and RNA are polynucleotides or long chains of nucleotides that are linked together. A nucleotide is...
    99.1K