Related Experiment Video

Updated: Jun 5, 2026

Modification and Functionalization of the Guanidine Group by Tailor-made Precursors
09:45

Modification and Functionalization of the Guanidine Group by Tailor-made Precursors

Published on: April 27, 2017

3α,6α-Bis(ethoxy-carbon-yl)glycoluril (diethyl 2,5-dioxoperhydro-imidazo[4,5-d]imidazole-3a,6a-dicarboxyl-ate)

Yu-Zhou Wang, Zhi-Guo Wang, Lin Li

    Acta Crystallographica. Section E, Structure Reports Online
    |January 5, 2011
    PubMed

    More Related Videos

    Chemical Inactivation of the E3 Ubiquitin Ligase Cereblon by Pomalidomide-based Homo-PROTACs10:44

    Chemical Inactivation of the E3 Ubiquitin Ligase Cereblon by Pomalidomide-based Homo-PROTACs

    Published on: May 15, 2019

    Preparation of Enantiopure Non-Activated Aziridines and Synthesis of Biemamide B, D, and epiallo-Isomuscarine11:04

    Preparation of Enantiopure Non-Activated Aziridines and Synthesis of Biemamide B, D, and epiallo-Isomuscarine

    Published on: June 13, 2022

    Related Concept Videos

    Preparation of Diols and Pinacol Rearrangement01:57

    Preparation of Diols and Pinacol Rearrangement

    Compounds bearing two hydroxyl groups are known as diols. When the hydroxyl groups are located on adjacent carbon atoms, the diols are called vicinal diols or glycols. Under acidic conditions, vicinal diols undergo a specific reaction called pinacol rearrangement.
    The reaction begins with transferring a proton from the acid catalyst to one of the hydroxyl groups, producing an oxonium ion.