Search Results - "Bentrude, Wesley G."

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    Trimethyl Phosphite as a Trap for Alkoxy Radicals Formed from the Ring Opening of Oxiranylcarbinyl Radicals. Conversion to Alkenes. Mechanistic Applications to the Study of C−C versus C−O Ring Cleavage by Ding, Bangwei, Bentrude, Wesley G

    Published in Journal of the American Chemical Society (19-03-2003)
    “…Trimethyl phosphite, (MeO)3P, is introduced as an efficient and selective trap in oxiranylcarbinyl radical (2) systems, formed from haloepoxides 8−13 under…”
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    Journal Article
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    A Facile Route to Vinyl- and Arylphosphonates by Vinyl and Aryl Radical Trapping with (MeO)3P by Jiao, Xian-Yun, Bentrude, Wesley G

    Published in Journal of organic chemistry (18-04-2003)
    “…The generation of vinyl or aryl radicals under classical, thermal AIBN/n-Bu3SnH conditions at 80 °C in the presence of an excess of (MeO)3P gives rise to the…”
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    Effect of Amino Substituents on the Stereochemical Outcome of the Photo-Arbuzov Rearrangements of 1-Arylethyl Phosphorodiamidites by Bhanthumnavin, Worawan, Bentrude, Wesley G

    Published in Journal of organic chemistry (10-06-2005)
    “…The essentially stereochemically pure 1-arylethyl phosphorodiamidites 8 and 9 were irradiated by UV light in acetonitrile, benzene, and cyclohexane (Tables…”
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    Photo-Arbuzov Rearrangements of 1-Arylethyl Phosphites:  Stereochemical Studies and the Question of Radical-Pair Intermediates by Bhanthumnavin, Worawan, Bentrude, Wesley G

    Published in Journal of organic chemistry (09-02-2001)
    “…The direct UV irradiation of the 1-arylethyl phosphites 7, 8, and 9 was carried out in acetonitrile, benzene, and cyclohexane, as was the…”
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    Free Radical Chain Reactions of [1.1.1]Propellane with Three-Coordinate Phosphorus Molecules. Evidence for the High Reactivity of the Bicyclo[1.1.1]pent-1-yl Radical by Dockery, Kevin P, Bentrude, Wesley G

    Published in Journal of the American Chemical Society (12-02-1997)
    “…Three-substituted bicyclo[1.1.1]pent-1-yl radicals (5), generated from additions of radicals to [1.1.1]propellane (1), are found to have high propensities to…”
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    Photo-Arbuzov Rearrangements of Benzylic Phosphites. Stereochemistry at Migratory Carbon by Bhanthumnavin, Worawan, Arif, Atta, Bentrude, Wesley G

    Published in Journal of organic chemistry (30-10-1998)
    “…The stereochemistry of the photo-Arbuzov rearrangement of the benzylic phosphite trans-(R,R‘)-10 to the corresponding phosphonate, 11, has been determined by…”
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    Laser Flash Photolysis Evidence for Styryl Radical Cation Cyclization in the SET-Induced Photorearrangement of a p-Methoxy-Substituted 2-Phenylallyl Phosphite by Shukla, Deepak, Lu, Cuong, Schepp, Norman P, Bentrude, Wesley G, Johnston, Linda J

    Published in Journal of organic chemistry (22-09-2000)
    “…The SET-induced photorearrangement of dimethyl 2-(4-methoxyphenyl)allyl phosphite, 9 (UV light, uranium glass filter, 9,10-dicyanoanthracene (DCA), biphenyl),…”
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    Photo-Arbuzov Rearrangements of Dimethyl Benzyl and Dimethyl p-Acetylbenzyl Phosphite by Ganapathy, Srinivasan, Soma Sekhar, B. B. V, Cairns, S. Matthew, Akutagawa, K, Bentrude, Wesley G

    Published in Journal of the American Chemical Society (17-03-1999)
    “…The direct ultraviolet irradiation of dimethyl benzyl phosphite (1) and dimethyl p-acetylbenzyl phosphite (8) was investigated in acetonitrile, cyclohexane,…”
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    SET-Induced Photorearrangement of 2-Phenylallyl Phosphites. Stereochemistry at Phosphorus. Application to Cyclic Nucleotide Derivatives by Hager, David C, Sopchik, Alan E, Bentrude, Wesley G

    Published in Journal of organic chemistry (05-05-2000)
    “…The stereochemistry at phosphorus of the SET-induced photorearrangement of diastereomeric 4-tert-butyl-2-phenylallyl-1,3,2-dioxaphosphorinanes (8) to the…”
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    Photo-Arbuzov rearrangements of cyclic phosphite systems by Landis, Margaret S, Turro, Nicholas J, Bhanthumnavin, Worawan, Bentrude, Wesley G

    Published in Journal of organometallic chemistry (01-03-2002)
    “…The direct UV irradiation of cyclic phosphites 1– 4 was carried out in argon-saturated solvents. In all cases examined, the rearranged, ring-contracted…”
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