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Disilazane, hexamethyl lithium derivative

The dimethyl tartrate derivative (144) forms the dilithium salt (145) with excess lithium hexamethyl-disilazane and this smoothly transforms into the butenolide (146), which is obtained crystalline in 78% yield.Lithiation of the hydroxy group prevents 1,2-elimination (Scheme 44). [Pg.827]


See other pages where Disilazane, hexamethyl lithium derivative is mentioned: [Pg.114]    [Pg.19]    [Pg.48]    [Pg.17]    [Pg.507]    [Pg.507]    [Pg.324]    [Pg.507]   
See also in sourсe #XX -- [ Pg.8 , Pg.19 ]

See also in sourсe #XX -- [ Pg.8 , Pg.19 ]

See also in sourсe #XX -- [ Pg.8 , Pg.19 ]

See also in sourсe #XX -- [ Pg.8 , Pg.19 ]

See also in sourсe #XX -- [ Pg.8 , Pg.19 ]




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2,2 ,4,4 ,5,5 -Hexamethyl

Disilazane, hexamethyl

Disilazanes

Lithium derivatives

Lithium, [1,1, 1,3,3,3-hexamethyl-2-

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