2018
DOI: 10.1134/s1070363218110075
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Reactions of Arylenedioxytrihalophosphoranes with Acetylenes: XV.1 Reaction of 2,2,2-Tribromo-4,6-di-tert-butylbenzo-1,3,2λ5-dioxaphospholedioxaphosphole with Pent-1-yne

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Cited by 4 publications
(2 citation statements)
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“…The diffraction data were collected on a Bruker D8 Venture photon diffractometer using graphite monochromated Mo Ka radiation (λ = 0.71073 Å). The structure was solved by direct methods using the SHELXL-2015 and SHELXL-2017 (Sheldrick, 2015 and Sheldrick, 2017) programs [17]. All of the non-hydrogen atoms were refined anisotropically and the hydrogen atoms were included in geometric positions but not refined.…”
Section: X-ray Diffraction Analysismentioning
confidence: 99%
“…The diffraction data were collected on a Bruker D8 Venture photon diffractometer using graphite monochromated Mo Ka radiation (λ = 0.71073 Å). The structure was solved by direct methods using the SHELXL-2015 and SHELXL-2017 (Sheldrick, 2015 and Sheldrick, 2017) programs [17]. All of the non-hydrogen atoms were refined anisotropically and the hydrogen atoms were included in geometric positions but not refined.…”
Section: X-ray Diffraction Analysismentioning
confidence: 99%
“…In subsequent papers, the electronic effect of donor and acceptor substituents at the arylacetylenes on the reaction rate was tested [69,70,71,72]. With the enhancement of the electron-donor properties of the substituent, the reaction rate increased.…”
Section: Synthesis and Some Reactions Of Alkyl 12-benzoxaphosphormentioning
confidence: 99%