Iodotriflamdation vs. Electrophilic Aromatic Iodination in the Reaction of N‐Phenyltriflamide with Alkenes
Author:
Affiliation:
1. A. E. Favorsky Irkutsk Institute of ChemistrySiberian Branch of Russian Academy of Sciences 664033 Irkutsk 1 Favorsky Street
Publisher
Wiley
Subject
General Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/slct.201801379
Reference21 articles.
1. Formation of 2,6-diphenyl-1,4-bis(trifluoromethylsulfonyl)piperazine in the reaction of styrene with trifluoromethylsulfonylnitrene
2. Formation of unexpected products in the attempted aziridination of styrene with trifluoromethanesulfonyl nitrene
3. Novel aziridination of olefins: direct synthesis from sulfonamides using t-BuOI
4. Oxidative addition of trifluoromethanesulfonamide to vinylcyclohexane and p-chlorostyrene
5. Reaction of trifluoromethanesulfonamide with alkenes and cycloocta-1,5-diene under oxidative conditions. Direct assembly of 9-heterobicyclo[4.2.1]nonanes
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2. New oxyalkyl derivatives of trifluoromethanesulfonamide: Dynamic rivalry between different types of chain and cyclic associates in different phase states;Journal of Molecular Structure;2020-11
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