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Alkylmagnesium chlorides

The position of the equilibrium depends upon the solvent and the identity of the specific organic group, but in ether lies well to the left for simple aryl-, alkyl-, and alkenylmagnesium halides.21 Solutions of organomagnesium compounds in diethyl ether contain aggregated species.22 Dimers predominate in ether solutions of alkylmagnesium chlorides. [Pg.623]

Preparative Methods phosphorus trichloride is allowed to react sequentially with alkylmagnesium chloride, methylmagnesium bromide, and BH3-THF complex in THF to give... [Pg.107]

Grignard Addition to Enones. The sultam generated from camphorsulfonic acid can also be used as a chiral auxiliary in the conjugate addition of Grignard reagents to enones. Simple alkylmagnesium chlorides add in a 1,4-fashion to afford imides (eq 19). ... [Pg.174]

Table 2. (EBTHI)Zr-catalyzed enantioselective carbomagnesation of unsaturated heterocycles with longer chain alkylmagnesium chlorides ... [Pg.420]

Table 4.7. (EBTHI) Zr-Calaly/cd Enantioscleetive Carbomagnesalion of Unsaluratcd Hctcrocyclcs with Longer Chain Alkylmagnesium Chlorides."... [Pg.118]

The reaction is carried out in ethereal solution it gives the best yields when alkylmagnesium chlorides are used the corresponding alkyl chlorides are by-products. The process has its main interest for preparation of primary amines whose amino group is attached to a secondary or tertiary carbon atom. Examples of its use and a tested. method of preparing chloramine are given in a review by Theilacker.1217 Also the unstable chloramine may be replaced by methoxylamine, which is easier to handle.1218... [Pg.548]

Reaction of alkylmagnesium chlorides with zinc methoxide in ether provides a highly valuable method to prepare salt-free dialkylzinc reagents, such as 34 or 35 (in ether solution [58] or solvent free [59]), that are otherwise difficult to obtain (Scheme 4.8). The approach takes advantage of the low solubility of magnesium methoxide in ether, which allows for its removal by filtration. [Pg.283]

Solutions of organomagnesium compounds in diethyl ether contain aggregated species. Dimers predominate in ether solutions of alkylmagnesium chlorides. The... [Pg.251]

Oppolzer W, Kingma AJ. Asymmetric induction on copper (I) chloride catalyzed 1,4-addition of alkylmagnesium chlorides to a,p-disubstituted ( )-enoylsultams and subsequent protonation. JSe/v. Chim. Acta 1989 72 1337-1345. [Pg.65]


See other pages where Alkylmagnesium chlorides is mentioned: [Pg.1045]    [Pg.956]    [Pg.956]    [Pg.112]    [Pg.154]    [Pg.138]    [Pg.545]    [Pg.682]    [Pg.85]    [Pg.204]    [Pg.83]    [Pg.44]    [Pg.4]    [Pg.191]    [Pg.181]    [Pg.49]    [Pg.274]    [Pg.682]    [Pg.4]    [Pg.191]    [Pg.144]    [Pg.222]    [Pg.389]    [Pg.82]    [Pg.408]    [Pg.234]   


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