@article{MoskalikShainyanSchilde2011,
  author    = {Moskalik, Mikail Yu. and Shainyan, Bagrat A. and Schilde, Uwe},
  title     = {Reaction of trifluoromethanesulfonamide with alkenes and cycloocta-1,5-diene under oxidative conditions direct assembly of 9-heterobicyclo[4.2.1]nonanes},
  series = {Russian journal of organic chemistry},
  volume    = {47},
  journal   = {Russian journal of organic chemistry},
  number    = {9},
  publisher = {Pleiades Publ.},
  address   = {New York},
  issn      = {1070-4280},
  doi       = {10.1134/S1070428011090016},
  pages     = {1271 -- 1277},
  year      = {2011},
  abstract  = {Reactions of trifluoromethanesulfonamide with alpha-methylstyrene, 2-methylpent-1-ene, and cycloocta-1,5-diene in the system t-BuOCl-NaI were studied. In the reaction with alpha-methylstyrene 1-iodo-2-phenylpropan-2-ol was the only isolated product. The reaction with 2-methylpent-1-ene gave a mixture of N,N'-(2-methylpentane-1,2-diyl)bis(trifluoromethanesulfonamide), trifluoro-N-(2-hydroxy-2-methylpentyl)-methanesulfonamide, and N,N'-[oxybis(2-methylpentan-2,1-diyl)]bis(trifluoromethanesulfonamide). Trifluoromethanesulfonamide reacted with cycloocta-1,5-diene to produce a mixture of 2,5-diiodo-9-(trifluoromethylsulfonyl)-9-azabicyclo[4.2.1]nonane and 2,5-diiodo-9-oxabicyclo[4.2.1]nonane; this reaction may be regarded as the first example of direct assembly of bicyclononane skeleton.},
  language  = {en}
}
@article{MeshcheryakovMoskalikKellingetal.2008,
  author    = {Meshcheryakov, Vladimir I. and Moskalik, Mikail Yu. and Kelling, Alexandra and Schilde, Uwe and Ushakov, Igor A. and Shainyan, Bagrat A.},
  title     = {Oxymethylation of trifluoromethanesulfonamide with paraformaldehyde in ethyl acetate},
  issn      = {1070-4280},
  doi       = {10.1134/S1070428008020206},
  year      = {2008},
  abstract  = {Acid-catalyzed reaction of trifluoromethanesulfonamide with paraformaldehyde in ethyl acetate led to the formation of oxymethylated products that did not form in the reaction carried out in sulfuric acid. Following products were obtained: 5-trifluoromethylsulfonyl-1,3-dioxazinane, 3,7-bis-(trifluoromethylsulfonyl)-1,5,3,7-dioxadiazocane, and a complex of trifluoromethanesulfonamide with 2,4,8,10-tetraoxospiro[5,5]undecene, 1:1. The spiroring resulted from the cyclization of pentaerythritol under the action of formaldehyde. The pentaerythritol formed in its turn by oxymethylation of the methyl group of ethyl acetate with paraformaldehyde followed by the reduction of the COOEt group into CH2 OH by the formaldehyde.},
  language  = {en}
}