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Ethylene glycol monobenzyl ether

The syntheses of di- and trifluoromethyl acyclonucleosides 634 are based on the substitution of the mesylates of the corresponding hemiacetals 633, obtained by condensing ethylene glycol monobenzyl ether with di- or triflu-oroacetaldehyde followed by mesylation. Their substitution by 2-amino-6-chloropurine or ALacetylcytosine gave 634, followed by hydrolysis and then hydrogenolysis (91TL3823). They were less active than acyclovir. [Pg.56]

Ethylene glycol monobenzyl ether (benzyl cellosolve) n. A solvent for cellulose acetate. [Pg.373]

Eosine YS 9713 1-Ethoxyhexane 5061 Ethylene glycol monobenzyl ether 817... [Pg.706]

See other pages where Ethylene glycol monobenzyl ether is mentioned: [Pg.314]    [Pg.65]    [Pg.482]    [Pg.141]    [Pg.529]    [Pg.166]    [Pg.2388]    [Pg.158]    [Pg.2546]    [Pg.86]    [Pg.2321]    [Pg.520]    [Pg.520]    [Pg.1719]    [Pg.1723]    [Pg.86]    [Pg.373]    [Pg.145]    [Pg.2165]    [Pg.189]    [Pg.2542]    [Pg.2490]    [Pg.177]    [Pg.188]    [Pg.2612]    [Pg.158]    [Pg.2324]    [Pg.2167]    [Pg.2173]   
See also in sourсe #XX -- [ Pg.86 , Pg.128 ]



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Ether ethylene

Ethylene glycol ethers

Glycols/glycol ethers

Monobenzylation

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