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  2. Riley oxidation - Wikipedia

    en.wikipedia.org/wiki/Riley_oxidation

    The Riley oxidation is a selenium dioxide-mediated oxidation of methylene groups adjacent to carbonyls. It was first reported by Harry Lister Riley and co-workers in 1932. [ 1 ] In the decade that ensued, selenium -mediated oxidation rapidly expanded in use, and in 1939, Andre Guillemonat and co-workers disclosed the selenium dioxide-mediated ...

  3. Organoselenium chemistry - Wikipedia

    en.wikipedia.org/wiki/Organoselenium_chemistry

    Selenium can exist with oxidation state −2, +2, +4, +6. Se(II) is the dominant form in organoselenium chemistry. Se(II) is the dominant form in organoselenium chemistry. Down the group 16 column, the bond strength becomes increasingly weaker (234 kJ / mol for the C−Se bond and 272 kJ/mol for the C−S bond) and the bond lengths longer ( C ...

  4. Selenium dioxide - Wikipedia

    en.wikipedia.org/wiki/Selenium_dioxide

    The selenium starting material is reduced to selenium, and precipitates as a red amorphous solid which can easily be filtered off. [10] This type of reaction is called a Riley oxidation. It is also renowned as a reagent for allylic oxidation, [11] a reaction that entails the following conversion Allylic oxidation. This can be described more ...

  5. Allyl group - Wikipedia

    en.wikipedia.org/wiki/Allyl_group

    The conversion of valencene to nootkatone is an example of allylic oxidation. In the synthesis of some fine chemicals, selenium dioxide is used to convert alkenes to allylic alcohols: [15] R 2 C=CR'-CHR" 2 + [O] → R 2 C=CR'-C(OH)R" 2. where R, R', R" may be alkyl or aryl substituents.

  6. Selenium compounds - Wikipedia

    en.wikipedia.org/wiki/Selenium_compounds

    Selenium forms two oxides: selenium dioxide (SeO 2) and selenium trioxide (SeO 3). Selenium dioxide is formed by the reaction of elemental selenium with oxygen: [5] + It is a polymeric solid that forms monomeric SeO 2 molecules in the gas phase. It dissolves in water to form selenous acid, H 2 SeO 3.

  7. Allyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Allyl_alcohol

    Allyl alcohols in general are prepared by allylic oxidation of allyl compounds, using selenium dioxide or organic peroxides. Other methods include carbon-carbon bond-forming reactions such as the Prins reaction, the Morita-Baylis-Hillman reaction, or a variant of the Ramberg-Bäcklund reaction. Hydrogenation of enones is another route.

  8. Selenium oxide - Wikipedia

    en.wikipedia.org/wiki/Selenium_oxide

    Selenium oxide may refer to either of the following compounds: Selenium dioxide, SeO 2; Selenium trioxide, SeO 3; Diselenium pentoxide, Se 2 O 5

  9. File:Seleniumdioxide oxidation.svg - Wikipedia

    en.wikipedia.org/wiki/File:Seleniumdioxide...

    Date/Time Thumbnail Dimensions User Comment; current: 09:15, 25 April 2011: 2,470 × 1,503 (47 KB): DMacks: convert text to paths in Inkscape (avoids WMF svg rendering bug when displayed in articles)