Related Experiment Video
Updated: Mar 21, 2026

Preparation of a Corannulene-functionalized Hexahelicene by CopperI-catalyzed Alkyne-azide Cycloaddition of Nonplanar Polyaromatic Units
Published on: September 18, 2016
Chemoselective [2+1] Cycloaddition of Difluorocarbene with Conjugated Enynes: Synthesis of Alkenyl
Zhongyi Wang1,2, Shuo Sun1, Chuanfa Ni1
1State Key Laboratory of Fluorine and Nitrogen Chemistry and Advanced Materials, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, 345 Ling-Ling Road, Shanghai 200032, China.
Abstract:
The chemoselective [2+1] cycloaddition of difluorocarbene with conjugated enynes has been achieved. Using TMSCF2Br as the difluorocarbene precursor in the presence of a catalytic amount of n-Bu4N+Br-, the reaction proceeded smoothly in THF at 110 °C, affording a series of alkenyl-substituted difluorocyclopropenes. Subsequently, these products could be hydrolyzed in one pot to furnish the corresponding alkenyl-substituted cyclopropenones.
More Related Videos
10:10Application of Elemental Lanthanides in the Selective C-F Activation of Trifluoromethylated Benzofulvenes Providing Access to Various Difluoroalkenes
Published on: July 28, 2018
12:27Synthesis of Hypervalent Iodonium Alkynyl Triflates for the Application of Generating Cyanocarbenes
Published on: September 8, 2013
Related Concept Videos
Cycloaddition Reactions: Overview
Electrophilic 1,2- and 1,4-Addition of X2 to 1,3-Butadiene
[4+2] Cycloaddition of Conjugated Dienes: Diels–Alder Reaction
Halogenation of Alkenes
Consider the bromination of cyclopentene. Molecular bromine is polarized in the proximity of the π electrons of cyclopentene. An electrophilic bromine atom adds across the double bond, forming a cyclic bromonium ion intermediate.
Cyclohexenones via Michael Addition and Aldol Condensation: The Robinson Annulation
Formation of Halohydrin from Alkenes