Halogen‐Induced Friedel‐Crafts Alkenylation Reactions with Haloalkynes: Direct Access to  gem ‐1, 1‐Dihaloalkenes | Zendy

Maji Biswajit | Zendy; Bhattacharya Aditya | Zendy; Hazra Sunit | Zendy

AI Assistant Blog Pricing

Home ZAIA Blog

Premium

Halogen‐Induced Friedel‐Crafts Alkenylation Reactions with Haloalkynes: Direct Access to gem ‐1, 1‐Dihaloalkenes

Author(s) -

Maji Biswajit,

Bhattacharya Aditya,

Hazra Sunit

Publication year - 2017

Publication title -

chemistryselect

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.437

H-Index - 34

ISSN - 2365-6549

DOI - 10.1002/slct.201702265

Subject(s) - friedel–crafts reaction , intramolecular force , aryl , halogen , chemistry , organic chemistry , combinatorial chemistry , catalysis , alkyl

A simple and efficient tactic for the synthesis of gem ‐hetero‐ or homo‐dihaloalkenes is reported from haloalkynes where Friedel‐Crafts alkenylation is a key step. The method provides functionalized tetrasubstituted alkenes which are important precursors in organic synthesis. The strategy is further extended with intramolecular Friedel‐Crafts alkenylation on ω ‐aryl alkynes to produce annulated arene carbocycles in a simple manner.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here

Accelerating Research