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Sulfate, cyclic

These reactions involve mosdy dimethyl and diethyl sulfate. Cyclic sulfates are also reactive, and several have been compared by determining reaction rates with a substituted pyridine or with water (40). In both cases, 1,2-ethylene sulfate is more reactive than 1,3-propylene sulfate or dimethyl or diethyl sulfates. [Pg.199]

See other pages where Sulfate, cyclic is mentioned: [Pg.846] [Pg.338] [Pg.243] [Pg.215] [Pg.231] [Pg.215] [Pg.231] [Pg.846] [Pg.2064] [Pg.2071] [Pg.2073] [Pg.2097] [Pg.2211] [Pg.2223] [Pg.2248] [Pg.2264] [Pg.2355] [Pg.2412] [Pg.2435] [Pg.2437] [Pg.2439] [Pg.2470] [Pg.2472] [Pg.2521] [Pg.2542] [Pg.2567] [Pg.2064] [Pg.2071] [Pg.2073] [Pg.2097]

See also in sourсe #XX -- [ Pg.369 ]

See also in sourсe #XX -- [ Pg.348 ]

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Aziridine sulfate cyclic

Chlorodeoxy sugars 2,3-cyclic sulfate

Cyclic Sulfates and Sulfites

Cyclic sulfate chemistry

Cyclic sulfates from 1,2-diols

Cyclic sulfates of 1,2-diols

Cyclic sulfates reactions

Cyclic sulfates ring opening reactions

Cyclic sulfates synthesis

Cyclic sulfates with nucleophiles

Cyclic sulfates, conversion

Diols cyclic sulfates

Glycol sulfates, cyclic

Glycols glycol sulfates, cyclic

Sugar sulfates cyclic

Sulfate esters cyclic

Sulfate esters, cyclic, preparation