Search Results - "Van De Water, Ryan W"

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  1. 1

    Synthesis of Resorcinol Derived Spironitronates by Marsini, Maurice A, Huang, Yaodong, Van De Water, Ryan W, Pettus, Thomas R. R

    Published in Organic letters (16-08-2007)
    “…Syntheses of several unique spironitronates are reported. The key transformation involves the first known example of an ipso oxidative cyclization of nitro…”
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    Journal Article
  2. 2

    Oxidative dearomatization of resorcinol derivatives: useful conditions leading to valuable cyclohexa-2,5-dienones by Van De Water, Ryan W, Hoarau, Christophe, Pettus, Thomas R.R

    Published in Tetrahedron letters (30-06-2003)
    “…The oxidative dearomatization of resorcinol derivatives with various oxidants is examined, as is the reactivity of cyclohexa-2,5-dienone that emerged. The…”
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  3. 3

    Regioselective Oxidation of Phenols to o-Quinones with o-Iodoxybenzoic Acid (IBX) by Magdziak, Derek, Rodriguez, Andy A, Van De Water, Ryan W, Pettus, Thomas R. R

    Published in Organic letters (24-01-2002)
    “…An efficient regioselective method for oxidation of phenols to o-quinones is reported. When this procedure is combined with a subsequent reduction, it proves…”
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  4. 4
  5. 5

    Synthesis of (±)-Epoxysorbicillinol Using a Novel Cyclohexa-2,5-dienone with Synthetic Applications to Other Sorbicillin Derivatives by Pettus, Liping H, Van De Water, Ryan W, Pettus, Thomas R. R

    Published in Organic letters (22-03-2001)
    “…A novel route to epoxysorbicillinol as well as dimers of sorbicillin is reported. The synthesis isin principleamenable to enantioselectivity. The key step is…”
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  6. 6
  7. 7

    A Mild Anionic Method for Generating o-Quinone Methides:  Facile Preparations of Ortho-Functionalized Phenols by Jones, Ryan M., Van De Water, Ryan W., Lindsey, Christopher C., Hoarau, Christophe, Ung, Thay, Pettus, Thomas R. R.

    Published in Journal of organic chemistry (18-05-2001)
    “…A low-temperature method for generating o-quinone methides is described which permits facile introduction of assorted R substituents onto the aryl ring system…”
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