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Azolinethiones, reactions

Azolines 13C NMR, 5, 20 H NMR, 5, 17 NMR, 5, 14 Azolinethiones reactions, 5, 102-103 Azolinones acidity, 5, 72 13C NMR, 5, 16, 19 H NMR, 5, 14, 15 halogenation, 5, 58 hydrolysis, 5, 64 IR spectra, 5, 24, 27 reactions, 5, 81 with aldehydes, 5, 60 with ketones, 5, 60 Azolin-2-ones electrophilic attack, 5, 99 Azolium cations nucleophilic attack at carbon, 5, 61 reactivity, 5, 42 Azolium ions reactions with alkali, 5, 63 with amines, 5, 65 Azolium salts hydrogen exchange, 5, 70 nucleophilic attack at hydrogen, 5, 69-72 reactions... [Pg.531]

Azolinones, azolinethiones, azolinimines N-Oxides, N-imides, N-ylides of azoles Thermal and Photochemical Reactions Formally Involving No Other Species 2.1 Thermal fragmentation... [Pg.39]

Many azolinethiones show reactions typical of thioamides in particular, they react with electrophiles at the sulfur atom. [Pg.102]

In another approach, the A((l)-y-hydroxypropyl isomer of (439) was cyclized in methanesulfonic acid <79CPB880>. Compounds (360)-(362) were formed (via the A -l-acylated intermediates) in high yields, as the only products in the reactions between the appropriate stereoisomeric quin-azolinethiones and acetylenedicarboxylate <89MRC959>. [Pg.693]


See other pages where Azolinethiones, reactions is mentioned: [Pg.531]    [Pg.531]    [Pg.864]    [Pg.531]    [Pg.531]    [Pg.531]    [Pg.864]    [Pg.531]    [Pg.1065]    [Pg.1065]    [Pg.375]    [Pg.375]   
See also in sourсe #XX -- [ Pg.458 ]




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