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Thiocarboxylates

The reaction of thioethers with ethyleneimine in the presence of acid yields sulfonium compounds. The reaction is reversible under alkaline conditions (125). Compounds in which double-bonded sulfur can exist in tautomerism with a form having a free SH group, such as thiourea (126,127), thiocarboxyhc acids (128), and thiophosphates (129), react to give aminoaLkylated products. The P-aminoethyl thiocarboxylate rearranges to give the amide. [Pg.5]

Mercapto Exist largely in the thione form Thiocarboxylic acid... [Pg.82]

Dewar and Turchi described the Comforth rearrangement of 5-alkoxyoxazole-4-thiocarboxylates as a potentially general method for the synthesis of 5-thiooxazole-4-carboxylic esters. Specifically, they found that thiol ester 13 underwent thermal isomerization to the corresponding 5-thiooxazole 14 in 94% yield. [Pg.226]

S-Alkylation of a thiocarboxylic acid with an a-halogenated carbonyl compound gives a thiol ester in which the two carbons to be connected... [Pg.132]

Liquid Crystals Containing Carboxylic or Thiocarboxylic Groups... [Pg.163]

Lewis TA, A Paszczynski, SW Gordon-Wylie, S Jeedigunta, C-H Lee, RL Crawford (2001) Carbon tetrachloride dechlorination by the bacterial transition metal chelator pyridine,2,6-bis(thiocarboxylic acid). Environ Sci Technol 35 552-559. [Pg.283]

Because of the higher reaction rate, 7V(3)-alkylimidazolium-A ( 1 )-carboxylates or thiocarboxylates have often been used for the synthesis of carbamates and thiocarbamates by the azolide method instead of imidazole-iV-carboxylates. [Pg.136]

With tetrazole-A-thiocarboxylate the amino group of an OH-protected deoxy-adenosine is converted into a thiocarbamate 189 ... [Pg.141]

Whereas CDI reacts with thiols to give thiocarboxylic imidazolide and the corresponding dithiocarbonate. The reaction with Nfl -sulfinyldiimidazole afforded, surprisingly, a mixture of dithio and trithio compounds in good yield [36]... [Pg.236]

O/S ligands, such as monothiocarbamates and thiocarboxylates, have been quite extensively characterized and some representative examples are discussed. [Pg.1223]

The complexes were shown to be monomeric in the solid state and have monodentate S-thiocarboxylate ligands. The thiocarboxylic anhydride elimination was studied by 1H and 13C NMR in solution, varying the R group and solvent.858... [Pg.1223]


See other pages where Thiocarboxylates is mentioned: [Pg.252]    [Pg.714]    [Pg.96]    [Pg.81]    [Pg.178]    [Pg.110]    [Pg.103]    [Pg.116]    [Pg.51]    [Pg.91]    [Pg.77]    [Pg.167]    [Pg.176]    [Pg.199]    [Pg.233]    [Pg.386]    [Pg.233]    [Pg.2444]    [Pg.140]    [Pg.192]    [Pg.237]    [Pg.1223]    [Pg.1047]    [Pg.1052]    [Pg.247]    [Pg.125]    [Pg.296]    [Pg.285]    [Pg.285]    [Pg.287]    [Pg.306]    [Pg.308]   
See also in sourсe #XX -- [ Pg.112 ]

See also in sourсe #XX -- [ Pg.3 , Pg.1305 ]




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Thiocarboxylation

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