Literature DB >> 20871880

Highly efficient two-step synthesis of (Z)-2-halo-1-iodoalkenes from terminal alkynes.

Zhengwang Chen1, Huanfeng Jiang, Yibiao Li, Chaorong Qi.   

Abstract

The easily accessible haloalkynes can be converted to (Z)-2-halo-1-iodoalkenes in high yields with excellent regio- and stereoselectivity. The method shows good functional group compatibility. The resulting products could find broad applications.

Entities:  

Year:  2010        PMID: 20871880     DOI: 10.1039/c0cc02156c

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  2 in total

1.  Regio- and Stereoselective Synthesis of 1,2-Dihaloalkenes Using In-Situ-Generated ICl, IBr, BrCl, I2, and Br2.

Authors:  Xiaojun Zeng; Shiwen Liu; Yuhao Yang; Yi Yang; Gerald B Hammond; Bo Xu
Journal:  Chem       Date:  2020-04-09       Impact factor: 22.804

2.  Hypervalent Iodine-Mediated Chemoselective Bromination of Terminal Alkynes.

Authors:  Youzhi Li; Xuemei Chen; Daya Huang; Zhenming Xie; Yan Liu
Journal:  Front Chem       Date:  2022-04-07       Impact factor: 5.545

  2 in total

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