Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Ylide compounds 1,3-thiazole derivatives

Phosphonium ylides 66 attack 1,2,4-dithiazole derivatives 65 (Y = 0, S) mainly at the S-S bond to give intermediates 67, which can either afford thiazoline derivatives 68 or react further, with a second ylide molecule 66 at the C=Y bond, to finally yield new thiazole and dithiole derivatives 69 and 70. Compounds 70 are predominant in this mixture (yields > 50%). They are oxidized into known dithiole derivatives 71 (Scheme 8) <1993MI33, 1994PS105, 1995PS63, 1999PS393>. [Pg.76]

Thiazole A -oxides, A -imides, and A -ylides are formally betaines derived from A -hydroxy-, A -amino-, and A -alkyl-azolium compounds. Where the cation is involved, reactivity is similar to that of thiazolium ions. [Pg.657]


See other pages where Ylide compounds 1,3-thiazole derivatives is mentioned: [Pg.180]    [Pg.160]    [Pg.167]    [Pg.180]    [Pg.180]    [Pg.180]    [Pg.423]    [Pg.249]    [Pg.315]    [Pg.15]   
See also in sourсe #XX -- [ Pg.339 , Pg.340 , Pg.341 , Pg.342 ]

See also in sourсe #XX -- [ Pg.339 , Pg.340 , Pg.341 , Pg.342 ]




SEARCH



Thiazole derivative

Ylide compounds derivations

Ylides compounds

© 2024 chempedia.info