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Titanium trichloromethyl

Thionyl chloride Thiophosgene Titanium tetrachloride Trichloromethyl perchlorate Triformoxime trinitrate Trimethylacetyl chloride Trimethylene glycol diperchlorate Trimethylol nitromethane trinitrate... [Pg.476]

Titanium fluoride (TlFg) F2Tli(g) 1111 Trichloromethyl (OCI3) CjClgCg) 559... [Pg.37]

Under certain circumstances, organochromium(ni) compoimds transfer their allaryl groups to aldehydes and, less frequently, to ketones. The particular selectivity and tolerance of this reaction make it particularly useful in organic synthesis. The use of these chromium reagents may be advantageous for use with acid-sensitive substrates, because of their reduced Lewis acidity relative to other transfer reagents [e.g., trichloromethyl-titanium(IV) or all[Pg.35]

SCHEME 43.51. A proposed mechanism of radical trichloromethylation of titanium enolates catalyzed by ruthenium(ll). [Pg.1331]

See other pages where Titanium trichloromethyl is mentioned: [Pg.237]    [Pg.1165]    [Pg.555]    [Pg.766]    [Pg.892]    [Pg.959]    [Pg.963]    [Pg.1036]    [Pg.852]    [Pg.857]    [Pg.861]    [Pg.1000]    [Pg.1006]    [Pg.1060]    [Pg.100]    [Pg.1330]   
See also in sourсe #XX -- [ Pg.16 , Pg.122 ]

See also in sourсe #XX -- [ Pg.16 , Pg.122 ]

See also in sourсe #XX -- [ Pg.16 , Pg.122 ]



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