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Modification of chemoselectivity and regioselectivity

Modification of Chemoselectivity and Regioselectivity 239 Tab. 5.2. Benzylation of 2-pyridone (31). Product distribution. [Pg.239]

Addition chemistry has developed into a promising tool for the modification and derivatization of the surface of nanotubes [24, 26], However, it is difficult to achieve chemoselectivity and regioselectivity control of addition reactions, requiring hot addends such as arynes, carbenes, radicals, nitrenes or halogens under drastic reaction conditions. [Pg.5]

See other pages where Modification of chemoselectivity and regioselectivity is mentioned: [Pg.233]    [Pg.233]    [Pg.235]    [Pg.243]    [Pg.249]    [Pg.251]    [Pg.261]    [Pg.233]    [Pg.233]    [Pg.235]    [Pg.243]    [Pg.249]    [Pg.251]    [Pg.261]    [Pg.161]    [Pg.381]    [Pg.49]    [Pg.40]    [Pg.31]    [Pg.125]    [Pg.551]   
See also in sourсe #XX -- [ Pg.233 , Pg.236 , Pg.241 , Pg.247 , Pg.253 , Pg.257 ]



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