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- 2,6-Dihalo-9-selenabicyclo[3.3.1]nonanes and their complexes with selenium dihalides: synthesis and structural characterisation. Vladimir A. Potapov, Svetlana V. Amosova, Elena V. Abramova, Maxim V. Musalov, Konstantin A. Lyssenko, M. G. Finn
, New J. Chem.
, 2015
, 39
, 8055
- The effect of leaving radical on the formation of tetrahydroselenophene by SH
i ring closure: an experimental and computational study. Amber N. Hancock, Sofia Lobachevsky, Naomi L. Haworth, Michelle L. Coote, Carl H. Schiesser
, Org. Biomol. Chem.
, 2015
, 13
, 2310
- Formal insertion of selenoketenes into donor–acceptor cyclopropanes: mesomeric alkynylselenolates as key starting materials. Anu Jacob, Peter G. Jones, Daniel B. Werz
, Org. Chem. Front.
, 2022
, 9
, 6933
- Syntheses of sulfur and selenium analogues of pachastrissamine
via double displacements of cyclic sulfate. Hongjun Jeon, Hoon Bae, Dong Jae Baek, Young-Shin Kwak, Deukjoon Kim, Sanghee Kim
, Org. Biomol. Chem.
, 2011
, 9
, 7237
- The [3 + 2] cycloaddition reaction of thiazole
carbene-derived C-C-Se 1,3-dipoles: a concise and highly efficient strategy for the construction of multifunctional dihydroselenophenes and selenopheno[2,3-b]pyrazines. Jian-Hong Zhang, Ying Cheng
, Org. Biomol. Chem.
, 2009
, 7
, 3264
- Homolytic substitution on selenium: formation of selenium-containing heterocycles by direct carbon–selenium bond formation. Carl H. Schiesser, Katarina Sutej
, J. Chem. Soc., Chem. Commun.
, 1992
, 57
- Fluxional characteristics of palladium(II) halide complexes of cyclic selenoethers. A dynamic nuclear magnetic resonance study. Edward W. Abel, Thomas E. MacKenzie, Keith G. Orrell, Vladimir Šik
, J. Chem. Soc., Dalton Trans.
, 1986
, 205
- Reductive cyclization of γ,δ-unsaturated selenothioic acid S-esters leading to tetrahydroselenophenes. Toshiaki Murai, Masahiko Maeda, Fumitake Matsuoka, Takahiro Kanda, Shinzi Kato
, Chem. Commun.
, 1996
, 1461
- The kinetics of alkyl radical ring closures at selenium: formation of selenane. Amber N. Hancock, Yvonne Kavanagh, Carl H. Schiesser
, Org. Chem. Front.
, 2014
, 1
, 645
- Synthesis and X-ray crystal structure of a selenophenoquinonoid-extended donor, BEDT–BDTS, affording highly conducting tetracyanoquinodimethaneand I3 complexes. Kazuko Takahashi, Takashi Shirahata, Kensuke Tomitani
, J. Mater. Chem.
, 1997
, 7
, 2375