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Tetraoxanes, synthesis

A practical synthesis has been claimed for the cycHc tetramer of formaldehyde, 1,3,5,7-tetraoxane [293-30-17, which has a boiling point of 175°C and a melting point of 112°C (155). It has found some use in textde treatment in Japan. [Pg.498]

As noted in the previous section, Vennerstrom and coworkers have carried out a large amount of research into the synthesis of tetraoxanes, e.g. 72, 73a and 73b, some of which have proven to be highly potent in For the synthesis of symmetrical... [Pg.1326]

General methods for the preparation of 1,2,4,5-tetraoxanes Key structures for the development of peroxidic antimalarial agents 12KGS60. Reactions oftetrazines with dienophiles 12KGS1237. 1,2,4,5-Tetrazines and azolo[l,2,4,5]tetrazines Synthesis and reactions with nucleophiles 13KGS75. [Pg.298]


See other pages where Tetraoxanes, synthesis is mentioned: [Pg.1457]    [Pg.1466]    [Pg.1492]    [Pg.1457]    [Pg.1466]    [Pg.1492]    [Pg.1280]    [Pg.1326]    [Pg.1280]    [Pg.1326]    [Pg.127]    [Pg.390]    [Pg.251]    [Pg.22]    [Pg.248]   
See also in sourсe #XX -- [ Pg.1317 , Pg.1318 , Pg.1332 ]




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Tetraoxanes

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