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Le Noble

Nitrobenzoic acid [552-16-9] M 167.1, m 146-148 , pK 2.21. Crystd from benzene (twice), n-butyl ether (twice), then water (twice). Dried and stored in a vacuum desiccator. [Le Noble and Wheland J Am Chem Soc 80 5397 1958.] Has also been crystd from EtOH/water. [Pg.310]

Facial selectivity of 5-substituted adamantan-2-ones (6) was initially studied by Giddings and Hudec [62], followed by intensive studies by le Noble s group [63-66]. Electron-withdrawing substituents such as phenyl (6b), fluoro (6c), hydroxyl and trifluoromethyl groups at the 5 position favored the syn addition... [Pg.133]

See other pages where Le Noble is mentioned: [Pg.33]    [Pg.33]    [Pg.174]    [Pg.174]    [Pg.796]    [Pg.942]    [Pg.304]    [Pg.304]    [Pg.304]    [Pg.304]    [Pg.307]    [Pg.465]    [Pg.89]    [Pg.246]    [Pg.259]    [Pg.302]    [Pg.580]    [Pg.581]    [Pg.587]    [Pg.604]    [Pg.605]    [Pg.605]    [Pg.606]    [Pg.640]    [Pg.1100]    [Pg.1100]    [Pg.1155]    [Pg.1253]    [Pg.1267]    [Pg.1360]    [Pg.1814]    [Pg.147]    [Pg.178]    [Pg.178]    [Pg.178]    [Pg.178]    [Pg.179]    [Pg.182]    [Pg.182]    [Pg.293]    [Pg.437]    [Pg.73]    [Pg.73]    [Pg.629]    [Pg.596]    [Pg.597]    [Pg.597]   
See also in sourсe #XX -- [ Pg.162 , Pg.172 ]



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Electrodeposition of less noble elements

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