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N-Methylcyclohexylamine

Carbons next to amine nitrogens are slightly deshielded in the NMR spectrum and absorb about 20 ppm downfield from where they would absorb in an alkane of similar structure. In N-methylcyclohexylamine, for example, the... [Pg.953]

N-Methylcyclohexylamine, 13C NMR spectrum of, 954 1H NMR spectrum of, 953 Methylene group, 178 N-Methylguanine, electrostatic potential map of, 1121 6-Methyl-5-hepten-2-ol, DRPT-NMR spectra of. 451... [Pg.1306]

C7H602 benzoic acid 65-85-0 9.274E-H09 65.370 12024 C7H15N N-methylcyclohexylamine 100-60-7 1.121E-H10 78.550... [Pg.654]

The Bsmoc derivative is formed from the chloroformate or the At-hydroxysuccin-imide ester. It is cleaved rapidly by aMichael addition with tris(2-aminoethyl)amine at a rate that leaves Fmoc derivatives intact. More hindered bases such as N-methylcyclohexylamine or diisopropylamine do not react with the Bsmoc group, but do cleave the Fmoc group, illustrating the importance of steric effects in additions to Michael acceptors. In the following example, Fmoc protection was unsuccessful because of purification problems associated with removal of the by-products from Fmoc deprotection. ... [Pg.715]

See other pages where N-Methylcyclohexylamine is mentioned: [Pg.963]    [Pg.1309]    [Pg.16]    [Pg.42]    [Pg.69]    [Pg.97]    [Pg.124]    [Pg.162]    [Pg.188]    [Pg.75]    [Pg.144]    [Pg.127]    [Pg.1808]    [Pg.114]    [Pg.35]    [Pg.233]    [Pg.459]    [Pg.567]    [Pg.666]    [Pg.114]    [Pg.595]    [Pg.1010]    [Pg.198]    [Pg.1006]    [Pg.1016]    [Pg.397]    [Pg.375]    [Pg.381]    [Pg.386]    [Pg.391]    [Pg.400]    [Pg.386]    [Pg.393]    [Pg.233]    [Pg.1010]   
See also in sourсe #XX -- [ Pg.415 ]

See also in sourсe #XX -- [ Pg.52 , Pg.127 ]

See also in sourсe #XX -- [ Pg.52 , Pg.127 ]

See also in sourсe #XX -- [ Pg.595 ]



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13C Nuclear magnetic resonance N-methylcyclohexylamine

N-METHYLCYCLOHEXYLAMINE.353(Vol

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