@article{PoleschnerHeydenreichSpindleretal.1994,
  author    = {Poleschner, Helmut and Heydenreich, Matthias and Spindler, Karla and Haufe, G.},
  title     = {Fluoroselenenylation of acetylenes with xenon difluoride/diorganyl diselenides and xenon difluoride/ phenylseleno trialkylsilanes},
  year      = {1994},
  language  = {en}
}
@article{PoleschnerHeydenreich1995,
  author    = {Poleschner, Helmut and Heydenreich, Matthias},
  title     = {13C NMR chemical shifts of unbranched 2-Alkyn-1-ols, w-Alkyn-1-ols and "internal" Alkyn-1-ols},
  year      = {1995},
  language  = {en}
}
@article{HeydenreichPoleschnerSchilde1996,
  author    = {Heydenreich, Matthias and Poleschner, Helmut and Schilde, Uwe},
  title     = {Fluoroselenenylation of Acetylenes with Xenon Difluoride-Diorganyl Diselenides : synthesis and structure elucidation of functionalized Vicinal (E)-Fluoro(organylseleno)olefins},
  year      = {1996},
  language  = {en}
}
@article{SchildePoleschner1996,
  author    = {Schilde, Uwe and Poleschner, Helmut},
  title     = {The first structure of a vicinal (E)-Fluoroselenoolefin: (E)-(5-Fluoro-4-octen-4-yl)dimethylselenonium Picrate},
  year      = {1996},
  language  = {en}
}
@article{PoleschnerHeydenreich1997,
  author    = {Poleschner, Helmut and Heydenreich, Matthias},
  title     = {1H and 13C NMR Spectra and One-Bond 13C,13C Coupling Constants of 2-Alken-4-yn-1-ols, (E)-2-Alken-4-yn-1-yl Acetates and (E)-2-Alken-4-yn-1-als},
  year      = {1997},
  language  = {en}
}
@article{PoleschnerHeydenreichSchilde2000,
  author    = {Poleschner, Helmut and Heydenreich, Matthias and Schilde, Uwe},
  title     = {13C, 19F and 77Se NMR study of vicinal (E)-fluoro(organylseleno)olefins and [(E)- fluoroalkenyl]diorganylselenonium salts},
  year      = {2000},
  abstract  = {Selenides of the type R1Se-EMe3 (E = Si, Ge, Sn, Pb) react with xenon difluoride by cleavage of the Se-E bond to yield the R1Se-F intermediate and the fluorides Me3E-F, whereas the Se-C bond in PhSe-tBu (E = C) is stable against XeF2. The presence of R1Se-F intermediates is confirmed by addition to acetylenes (4-octyne, 3-hexyne). Thus, the fluoroselenenylation of acetylenes gives fluoro(organylseleno)olefins in preparative yields. In the cases of E = Si, Ge, Sn, and Pb, aryl and n-alkyl groups are suitable as the substituent R1. The X-ray crystal structural analysis of (E)-3- (p-carboxyphenylseleno)-4-fluorohex-3-ene - the first example of an uncharged fluoroselenoolefin synthesized from p- EtO2C-C6H4-Se-SnMe3, XeF2, and 3-hexyne followed by an ester hydrolysis - shows that the addition of the selenenylfluoride intermediate to the acetylene proceeds via a trans-addition, as is known for the R2Se2-XeF2 reagents.},
  language  = {en}
}