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Bromine-zinc exchange

Numerous modifications of the direct zinc insertion procedure can be found in the hterature. For example, simple diaUcylzincs can be used as reagents instead of metallic Zn, bnt in this case the reaction is accelerated by catalytic qnantities of zinc salts or transition metal see Transition Metals) salts. Whereas the Cu -catalyzed iodine-zinc exchange reaction provides diorganozincs, the Pd, Mn and nF catalyzed iodine- or bromine-zinc exchange leads to organozinc halides. [Pg.5212]

Bromine-zinc exchange. MnBr2 together with Cul catalyzes the exchange, thus rendering the preparation of RZnBr from RBr and Et2Zn quite readily in DMPU at room temperature. [Pg.230]

The above-mentioned method is applied to the selective carbon-carbon bond formation between sp carbons [150]. A bromine-zinc exchange reaction of the gcm-dibromo-cyclopropane 96 selectively occurs at the position cis to the phenyl group by treatment with Me4ZnLi2 [151], The reaction of the thus-obtained zincate 97 with VO(OEt)Cl2 leads to the stereoselective formation of l-bromo-l-methyl-2-phenylcyclopropane (98). On the other hand, when the reaction mixture is wanned up to 0 °C, followed by treatment with VO(OEt)Cl2, dimelhylation at the em-positions takes place to give the dimethylcyclopropane (100) via the organozinc 99 as shown in Scheme 2.79)... [Pg.37]

Harada T, Katsuhira T, Oku A (1992) Stereochemistry in carbenoid formation by bromine/ lithium and bromine/zinc exchange reactions of 1,1-dibromoalkenes higher reactivity of the sterically more hindered bromine atom. J Org Chem 57 5805-5807. doi 10.1021/jo00048a002... [Pg.199]

The synthesis of 6-deoxy-D-glucose (see D-Quinovose, p, 99) is carried out from 2,3,4-tri-0-acetyl-6-bromo-6-deoxy-a-D-glucosyl bromide. The dihalide is converted to the methyl 2,3,4-tri-0-acetyl-6-bromo-6-deoxy-i -D-glucoside by treatment with silver carbonate and methyl alcohol, and the bromine is exchanged for a hydrogen atom by reduction with zinc and acetic acid 227). [Pg.130]

The bromine-metal exchange in a-bromo carbonyl compounds is a common method for the formation of zinc enolates - a procedure whereupon the well-known Reformatsky reaction is based [159]. The question whether zinc enolates feature a carbon-zinc or an oxygen-zinc bond seems to depend on the individual... [Pg.63]

Zinc is electrodeposited from the sodium zincate electrolyte during charge. As in the zinc/bromine battery, two separate electrolytes loops ("posilyte" and "nega-lyte") are required. The only difference is the quality of the separator The zinc/ bromine system works with a microporous foil made from sintered polymer powder, but the zinc/ferricyanide battery needs a cation exchange membrane in order to obtain acceptable coulombic efficiencies. The occasional transfer of solid sodium ferrocya-nide from the negative to the positive tank, to correct for the slow transport of complex cyanide through the membrane, is proposed [54],... [Pg.206]


See other pages where Bromine-zinc exchange is mentioned: [Pg.351]    [Pg.597]    [Pg.689]    [Pg.695]    [Pg.697]    [Pg.702]    [Pg.78]    [Pg.102]    [Pg.186]    [Pg.221]    [Pg.335]    [Pg.64]    [Pg.351]    [Pg.597]    [Pg.689]    [Pg.695]    [Pg.697]    [Pg.702]    [Pg.78]    [Pg.102]    [Pg.186]    [Pg.221]    [Pg.335]    [Pg.64]    [Pg.252]    [Pg.303]    [Pg.688]    [Pg.106]    [Pg.115]    [Pg.93]    [Pg.252]    [Pg.204]    [Pg.94]    [Pg.128]    [Pg.91]    [Pg.232]    [Pg.304]    [Pg.4]    [Pg.29]    [Pg.25]    [Pg.397]    [Pg.72]    [Pg.223]    [Pg.784]    [Pg.298]    [Pg.955]    [Pg.88]    [Pg.264]    [Pg.955]    [Pg.50]   
See also in sourсe #XX -- [ Pg.102 , Pg.186 ]

See also in sourсe #XX -- [ Pg.230 ]




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Bromine-zinc exchange reactions

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