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Lodosobenzene diacetate

De Armas, P., Carrau, R., Concepcion, J. I., Francisco, C. G., Hernandez, R., Suarez, E. Synthesis of 1,4-epimine compounds, lodosobenzene diacetate, an efficient reagent for neutral nitrogen radical generation. Tetrahedron Lett. 1985, 26, 2493-2496. [Pg.602]

Camps, P., Lukach, A. E., Pujol, X., Vazquez, S. Hunsdiecker-type bromodecarboxylation of carboxylic acids with lodosobenzene diacetate-bromine. Tetrahedron 2000, 56, 2703-2707. [Pg.606]

Comparison with lead tetraacetate, lodosobenzene diacetate cleaves e/c-glycols in acetic acid at 50-80° but the rate constant is about one hundredth that of lead tetraacetate. - Further analogies to lead tetraacetate are that the reagent is capable of converting olefins into glycol diacetates" and that on decomposition in refluxing acetic acid containing 2,4,6-trinitrotoluene this substrate is methylated to trinitro-m-xylene to the extent of about 20%. ... [Pg.257]

See other pages where Lodosobenzene diacetate is mentioned: [Pg.116]    [Pg.219]    [Pg.335]    [Pg.384]    [Pg.385]    [Pg.586]    [Pg.606]    [Pg.257]    [Pg.257]    [Pg.257]    [Pg.988]    [Pg.1390]    [Pg.32]    [Pg.33]    [Pg.33]    [Pg.99]    [Pg.181]    [Pg.5]    [Pg.364]    [Pg.290]    [Pg.319]    [Pg.183]    [Pg.183]    [Pg.106]    [Pg.355]    [Pg.263]    [Pg.377]    [Pg.290]    [Pg.2266]   


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Lodosobenzene

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