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Dimethy If ormamide

Aprotic solvents are not protogenic, but can be protophilic, e.g. acetone, 1,4-dioxan, tetrahy drof uran, dimethy If ormamide, hexamethylphos-phortriamide, propylene carbonate and sulpholane. Solvents that do not participate in protolytic reactions, i.e. do not donate or accept a proton, are usually chemically inert, such as benzene, chlorobenzene, chloroform, tetrachloromethane, etc. [Pg.58]

Anhydrotetracycline stock solution 2mgmL 1 anhydrotetracycline (Acros) in N, N-dimethy If ormamide. [Pg.37]

A mixture of 3a-acetoxy-5-hydroxy-7a-bromo-5a-cholestan-6-one and anhydrous LiBr in dimethy If ormamide heated 18 hrs. at ca. 80° 3a-acetoxy-5-hydroxy-7/5-bromo-5a-cholestan-6-one. Y 77%. F. e. s. A. T. Rowland, R. S. Drawbaugh, and J. R. Dalton, J. Org. Chem. 42, 487 (1977). [Pg.424]


See other pages where Dimethy If ormamide is mentioned: [Pg.450]    [Pg.483]    [Pg.330]    [Pg.493]    [Pg.473]    [Pg.450]    [Pg.483]    [Pg.330]    [Pg.493]    [Pg.473]   
See also in sourсe #XX -- [ Pg.24 , Pg.26 , Pg.33 , Pg.34 , Pg.119 , Pg.123 , Pg.192 , Pg.206 , Pg.230 , Pg.236 , Pg.251 , Pg.269 , Pg.274 , Pg.298 , Pg.327 , Pg.370 , Pg.441 , Pg.445 , Pg.446 , Pg.448 , Pg.504 , Pg.505 , Pg.558 , Pg.562 , Pg.575 ]




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