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Aluminum bis

Methylaluminum bis(4-bromo-2,6-di-tert-butyiphenoxide) Aluminum, bis[4-bromo-2,6-bis(1,1-dimethylethyl)phenolato]methyl- (12) (118495-99-1)... [Pg.204]

C64H82AIBN2O4, Aluminum, bis(tetrahydrofur-an)-l,2-bis(2-hydroxy-3,5-bis(tert-butyl)-benzyhdeneimino)ethane-, tetraphenylborate, 34 19... [Pg.245]

Butylmagnesium bromide-Methyl-aluminum bis(2,6-di-/-butyl-4-methyl-phenoxide), 203... [Pg.405]

Diisobutyl(iodomethyl)aluminum, 114 Dimethylaluminum chloride, 5 Ethylaluminum dichloride, 5, 44, 306 Ethylmagnesium bromide-Methyl-aluminum bis(2,4,6-tri-r-butyl-phenoxide), 203 Isobutyl(2,4,6-tributylphenoxy)-aluminum trifluoromethanesulfonate, 113... [Pg.406]

Fig. 13. Molecular structure of [Me3SiOAl(BH4)2]2, dimeric trimethylsilyloxy-aluminum-bis(tetrahydroborate) [33]... Fig. 13. Molecular structure of [Me3SiOAl(BH4)2]2, dimeric trimethylsilyloxy-aluminum-bis(tetrahydroborate) [33]...
The choice of Lewis acid promoter for these reactions can change the sense of asymmetric induction. " For example, tandem [4 + 2]/ [3 + 2] cycloadditions (eq 4) mediated by Ti(0-i-Pr)2Cl2, followed by hydrogenolysis afforded tricyclic (-)-a-hydroxy lactam [(-)-8] in 98% ee. When mediated by methyl-aluminum-bis(2,6-diphenylphenoxide) (MAPh), the same reaction gave (+ )-8 in 93% ee. Importantly, the observed selectivity is not chiral auxiliary dependent. Rather, it is attributed to a highly endo selective cycloaddition in the case of Ti compared to high exo selectivity in the case of MAPh. [Pg.297]

Aluminum tris(2,6-diplienylphenoxide) (ATPH), an aluminum-based Lewis acid with bulky substituents, is valuable as an extremely selective activator of less hindered aldehyde carbonyls (Scheme 10.8) [36]. In competitive aldol reactions of two different aldehydes, more fhan one equivalent of ATPH achieves highly chemoselective functionalization of less hindered aldehydes. Unfortunately, catalytic use of ATPH reduces the chemical yield and chemoselectivity. In contrast, a catalytic quantity of aluminum bis(trifluoromethanesulfonyl)amide 13 can promote the chemoselective aldol reaction. [Pg.414]

Aluminum bis-(N-methylpiperazino)hydride, obtained by combining 2 equivalents of N-methylpiperazine and a solution of AIH3 in THF, is especially recommended for the reduction of esters or acids to aldehydes (Sections 3.2.5, 3.2.6) [MM3]. [Pg.14]

The first example of this type of living-radical polymerization was reported by Sawamoto, who used a ruthenium metal complex in association with methyl-aluminum bis(2,6-di- ert-butylphenoxide), as an accelerator, to polymerize methyl... [Pg.482]

CAS 142-03-0 EINECS/ELINCS 205-518-2 Synonyms Aluminum acetate Aluminum acetate basic Aluminum, bis (acetato-0) hydroxy- Aluminum diacetate hydroxide Aluminum hydroxyacetate Aluminum subacetate Basic aluminum acetate Bis (acetato-O) hydroxyaluminum Hydroxy aluminum diacetate Mordant rouge Classification Salt Empirical C4H7AIO5 Formula AI(0H)(CH3C02)2 Properties Wh. amorphous powd. insol. in water sol. in water if freshly prepared forming acidic sol ns. m.w. 162.08 m.p. 54 C Toxicology Skin irritant... [Pg.184]


See other pages where Aluminum bis is mentioned: [Pg.81]    [Pg.110]    [Pg.276]    [Pg.84]    [Pg.38]    [Pg.102]    [Pg.84]    [Pg.92]    [Pg.113]    [Pg.137]    [Pg.110]    [Pg.709]    [Pg.55]    [Pg.580]    [Pg.180]    [Pg.97]    [Pg.14]    [Pg.123]   
See also in sourсe #XX -- [ Pg.17 , Pg.37 ]




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Aluminum Catalysts from Axially Chiral Bis-Phenols

Aluminum Catalysts from Bis-Sulfonamides

Aluminum hydride, bis reduction

Aluminum hydride, bis reduction amides

Aluminum hydride, bis reduction enones

Aluminum tris[2,6-bis

Aluminum, bis hydrido

Aluminum, diaqua-1,2-bis

Aluminum, dimethanol-l,2-bis ethane

Bis aluminum hydride

Lithium aluminum hydride-Bis nickel

Methyl aluminum bis

Sodium bis aluminum

Sodium bis aluminum hydride

Sodium bis aluminum hydride a-siloxy ketones

Sodium bis aluminum hydride alcohols

Sodium bis aluminum hydride aldehydes

Sodium bis aluminum hydride allylic alcohol synthesis

Sodium bis aluminum hydride amides

Sodium bis aluminum hydride aromatic nitriles

Sodium bis aluminum hydride benzylic halides

Sodium bis aluminum hydride carbonyl compounds

Sodium bis aluminum hydride carboxylic acids

Sodium bis aluminum hydride epoxides

Sodium bis aluminum hydride esters

Sodium bis aluminum hydride imines

Sodium bis aluminum hydride lactones

Sodium bis aluminum hydride pyridines

Sodium bis aluminum hydride reduction

Thallium bis borate, complex with aluminum

Thallium bis borate, complex with aluminum and gallium alkyls

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