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TEBAC

TEBAC = Et3N CH2Ph Cl General Cleavage of Esters... [Pg.229]

TMBAC, tnmethylbenzylammomum chlonde, RT, room temperature, TEBAC, tnethylbenzylammomum chlonde... [Pg.775]

Another modern modification involves coupling of UNs 30 and /1-ketoesters 36 in aqueous emulsion in the presence of an interphase catalyst triethylbenzylammonium chloride (TEBAC) (06JCM228). [Pg.190]

Recently, reactions of cyclic diketones 103 with UNs were carried out via solvent-free ball-milling of starting materials at 100-130°C (03T3753) or at room temperature in the presence of TEBAC (06SC2363) with nearly quantitative yields. [Pg.203]

Triazole is reported to give charged polymers (31) on reaction with 1,4-dichlorobut-2-ene, KOH and TEBAC in dioxane. Under controlled conditions 1,4-bis(A -triazolyl)-but-2-ene can be obtained <89CHE414>. [Pg.137]

A R4CH2X, Cs2C03, DMF B R4CH2X, solid K2C03, TEBAC... [Pg.221]

CH2FCH(OH)(CF2)7CF3 50% NaOH 2-(2-chloroethyl)-oxiraile, TEBAC, 25CC, 4 h R F 17 66 58... [Pg.355]

See other pages where TEBAC is mentioned: [Pg.229]    [Pg.484]    [Pg.775]    [Pg.775]    [Pg.775]    [Pg.776]    [Pg.1307]    [Pg.1307]    [Pg.376]    [Pg.801]    [Pg.303]    [Pg.113]    [Pg.224]    [Pg.250]    [Pg.79]    [Pg.79]    [Pg.309]    [Pg.385]    [Pg.855]    [Pg.898]    [Pg.251]    [Pg.221]    [Pg.223]    [Pg.354]    [Pg.355]    [Pg.355]    [Pg.355]    [Pg.775]    [Pg.775]    [Pg.775]    [Pg.776]    [Pg.1307]    [Pg.1307]    [Pg.457]    [Pg.563]    [Pg.184]    [Pg.185]    [Pg.427]    [Pg.427]    [Pg.6]    [Pg.364]    [Pg.124]   
See also in sourсe #XX -- [ Pg.855 ]

See also in sourсe #XX -- [ Pg.855 ]



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TEBAC chloride

Triethylbenzylammonium chloride TEBAC)

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