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Selective 1,2-dihalogenation and oxy-1,1-dihalogenation of alkynes by N-halosuccinimides

Authors :
Liu, Jinhua
Li, Wenjuan
Wang, Chao
Li, Yao
Li, Zhiping
Source :
Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry. Aug2011, Vol. 52 Issue 33, p4320-4323. 4p.
Publication Year :
2011

Abstract

Abstract: 1,2-Dihalogenation and oxy-1,1-dihalogenation of alkynes by N-halosuccinimides can be selectively realized through using different reaction conditions. α,β-Dihalo alkenes were obtained exclusively using THF as solvent without using any catalyst, while α,α-dihalo ketones were synthesized using a mixed solvent of THF and H2O in the presence of FeCl3·6H2O. Terminal aromatic alkynes are smoothly transformed into α,α-dihalo ketones on water without a catalyst. [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
00404039
Volume :
52
Issue :
33
Database :
Academic Search Index
Journal :
Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry
Publication Type :
Academic Journal
Accession number :
62843088
Full Text :
https://doi.org/10.1016/j.tetlet.2011.06.047