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Diiodomethane-Zinc-Titanium chloride

Butyllithium-Potassium f-butoxide, 56 Diiodomethane-Zinc-Titanium(IV) chloride, 114... [Pg.392]

Related Reagents. Dibromomethane-Zinc-Titanium(IV) Chloride Diiodomethane-Zinc-Titanium(IV) Chloride 4R, 5i )-2,2-Dimethyl-4,5-bis(hydroxydiphenylmethyl)-l,3-di-oxolane-Titanium(IV) Chloride Lithium Aluminum Hydride-Titanium(IV) Chloride Titanium(IV) Chloride-Diazabicyclo-[5.4.0]undec-7-ene Titanium(IV) Chloride-2,2,6,6-Tetramethyl-piperidine Titanium(IV) Chloride-Triethylaluminum Titanium-(IV) Chloride-Zinc. [Pg.388]

Diethylzinc-Titanium(IV) chloride, 21 Diiodomethane-Diethylzinc, 276 Diiodomethane-Zinc-copper couple, 275... [Pg.416]

An equimolar mixture of 4 and jS-TiCh generated reactive spedes for the methylenation, as shown in Table 5.2. As described above, the methylenation procedure due to Takai or Lombardo employed diiodomethane, zinc, and titanium(IV) chloride. In these procedures, the titanium(IV) chloride would be reduced to titanium(O), titanium(I), titanium(II), or titanium(III). The oxidation state of tita-... [Pg.206]

Nozaki, Oshima, and Takai reported in 1978 that the reagent prepared from diio-domethane, zinc, and titanium(IV) chloride was effective for the methylenation of ketones [12]. In this procedure, a reagent was prepared by mixing diiodomethane (3.0 equiv.), zinc dust (9.0 equiv.), and titanium(IV) chloride (1.0 equiv.) in THF for 30 min at 25 °C. The ketone substrate (1.0 equiv.) was then added to the prepared reagent. Other metal halides were also examined (Scheme 5.5), but none of them gave better results than titanium) IV) chloride. [Pg.203]


See other pages where Diiodomethane-Zinc-Titanium chloride is mentioned: [Pg.368]    [Pg.381]    [Pg.416]    [Pg.644]    [Pg.653]    [Pg.280]    [Pg.349]    [Pg.205]   
See also in sourсe #XX -- [ Pg.114 ]

See also in sourсe #XX -- [ Pg.114 ]

See also in sourсe #XX -- [ Pg.388 ]




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Diiodomethane

Titanium chloride

Titanium chloride-Zinc

Zinc chloride

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