Perfluoroalkylation of alkenes and alkynes in water
Perfluoroalkylation of alkenes and alkynes was performed using thermal initiation by ACCN (1,1′-azobis(cyclohexanecarbonitrile)) in water, with good yields. The procedure is simple and more ecofriendly that most of the methods published for the synthesis of related compounds. Using water (without an...
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todo:paper_15517004_v2015_n5_p190_Vazquez2023-10-03T16:25:21Z Perfluoroalkylation of alkenes and alkynes in water Vázquez, A.J. Nudelman, N.S. Perfluoroalkylation Radical addition Reactions in water Thermal initiation Perfluoroalkylation of alkenes and alkynes was performed using thermal initiation by ACCN (1,1′-azobis(cyclohexanecarbonitrile)) in water, with good yields. The procedure is simple and more ecofriendly that most of the methods published for the synthesis of related compounds. Using water (without any cosolvent or metal catalysts), it allows the synthesis of the addition products with medium to high yields. ©ARKAT-USA, Inc. Fil:Vázquez, A.J. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_15517004_v2015_n5_p190_Vazquez |
institution |
Universidad de Buenos Aires |
institution_str |
I-28 |
repository_str |
R-134 |
collection |
Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) |
topic |
Perfluoroalkylation Radical addition Reactions in water Thermal initiation |
spellingShingle |
Perfluoroalkylation Radical addition Reactions in water Thermal initiation Vázquez, A.J. Nudelman, N.S. Perfluoroalkylation of alkenes and alkynes in water |
topic_facet |
Perfluoroalkylation Radical addition Reactions in water Thermal initiation |
description |
Perfluoroalkylation of alkenes and alkynes was performed using thermal initiation by ACCN (1,1′-azobis(cyclohexanecarbonitrile)) in water, with good yields. The procedure is simple and more ecofriendly that most of the methods published for the synthesis of related compounds. Using water (without any cosolvent or metal catalysts), it allows the synthesis of the addition products with medium to high yields. ©ARKAT-USA, Inc. |
format |
JOUR |
author |
Vázquez, A.J. Nudelman, N.S. |
author_facet |
Vázquez, A.J. Nudelman, N.S. |
author_sort |
Vázquez, A.J. |
title |
Perfluoroalkylation of alkenes and alkynes in water |
title_short |
Perfluoroalkylation of alkenes and alkynes in water |
title_full |
Perfluoroalkylation of alkenes and alkynes in water |
title_fullStr |
Perfluoroalkylation of alkenes and alkynes in water |
title_full_unstemmed |
Perfluoroalkylation of alkenes and alkynes in water |
title_sort |
perfluoroalkylation of alkenes and alkynes in water |
url |
http://hdl.handle.net/20.500.12110/paper_15517004_v2015_n5_p190_Vazquez |
work_keys_str_mv |
AT vazquezaj perfluoroalkylationofalkenesandalkynesinwater AT nudelmanns perfluoroalkylationofalkenesandalkynesinwater |
_version_ |
1807320014456356864 |