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Adipic 3,4-dichloro

Dichlorophenoxy acetic acid (2,4-D) Di(2-ethylhexyl)adipate 2,6-Dichloro-4-phenylenediamine ... [Pg.219]

Various cyclitols (and acyclic polyols) have been desynunetrized by formation of dispoke intermediates. (See for example, Vol. 28, p. 237, ref. 115). L-Chiro-inositol can be converted to the silyl derivative 67 in which the trans-diol units are protected on reaction with l,3-dichloro-l,l,3,3-tetraisopropylidisiloxane (TipsQ). Compound 67 was further converted into conduritol B epoxide and its thioepoxide analogue. The conversion of some tetra-O-substituted myo-inosi-tols into adipic dialdehyde derivatives is mentioned in Chapter IS. [Pg.239]


See other pages where Adipic 3,4-dichloro is mentioned: [Pg.302]    [Pg.31]    [Pg.41]    [Pg.236]    [Pg.99]    [Pg.255]    [Pg.377]   
See also in sourсe #XX -- [ Pg.178 ]




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