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Alkyl-substituted alkynyl substrates

After this seminal work, the alkynylation reaction with alkynyliodonium salts was applied to several classes of substrates, including diketones [36-38], ketoesters [36], malonates [36, 39], and aminomalonates [40, 41], The latter class of compounds is especially interesting, as it was also successful in the case of alkyl substituted alkynes. This was probably made possible by an efficient 1,2-shift of the nitrogen heteroatom. [Pg.192]


See other pages where Alkyl-substituted alkynyl substrates is mentioned: [Pg.51]    [Pg.51]    [Pg.72]    [Pg.72]    [Pg.505]    [Pg.549]    [Pg.17]    [Pg.215]    [Pg.254]    [Pg.13]    [Pg.1052]    [Pg.46]    [Pg.281]    [Pg.69]    [Pg.1230]    [Pg.651]    [Pg.205]    [Pg.69]    [Pg.278]    [Pg.716]    [Pg.92]    [Pg.445]    [Pg.92]    [Pg.445]    [Pg.92]    [Pg.445]    [Pg.374]    [Pg.607]    [Pg.493]    [Pg.153]    [Pg.1613]    [Pg.298]    [Pg.651]   
See also in sourсe #XX -- [ Pg.51 ]




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