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Potassium thiobenzoate

Potassium 4-chloro-3,5-dinitrobenzene-sulfonate, 31, 46 Potassium cyanate, 31, 9 Potassium cyanide, 30,84 32,31,63 37,47 Potassium ethyl malonate, 37, 34 Potassium ethyl xanthate, 30, 56 Potassium fluoride, 36, 40 Potassium iodide, 30, 34 31, 31, 66 Potassium metal, 37, 29, 30 Potassium methyl sulfate, 31, 73 Potassium nitrate, 31, 46 Potassium 1-nitropropylnitronate, 37, 24 Potassium oxalate, 34, 83 Potassium permanganate, 30, 87 31, 59 Potassium sulfide, 32, 103 Potassium thiobenzoate, 32, 101 Potassium thiocyanate, 32, 39, 40 Prins reaction, 33, 72 Propane, 1, 3-dibromo-2, 2-Ws-(bromo-methyl)-, 31, 82... [Pg.53]

The Pd-catalyzed allylic alkylation of thiocarboxylate ions was carried out with potassium thioacetate (KSAc) and potassium thiobenzoate (KSBz) and the racemic cyclic and acyclic carbonates rac-3aa, rac-3ba, rac-lda, rac-laa, rac-lba, and rac-lca, respectively (Scheme 2.1.4.21). The carbonates rac-3aa, rac-3ba, rac-lda, rac-laa, and rac-lba were treated with KSAc (1.4 equiv) or KSBz (2.0 equiv) in the presence of Pd(0)/L (2 mol%) and BPA (8 mol%) in CH2CI2/H2O. Under these conditions the acyclic carbonates rac-3aa and rac-3ba gave the thioesters 18aa, 18ab and 18ba, respectively (Table 2.1.4.14, entries 1-3), with high enantioselec-tivities in high yields [26]. [Pg.234]

Reist and coworkers [9,10] described the first sulfur-containing furanose rings. They prepared 4-thio-D-ribofuranose 14 (Figure 9.4) and 4-thio-L-ribofuranose via nucleophihc displacement of the tosylate in 2,3-(9-isopropylidene-4-(9-toluenesulfonyl-a-D- and -a-L-lyxopyranosides, respectively, with potassium thiobenzoate in DMF. Several nucleosides of 4-thiofuranoses were subsequently synthesized. For example, the 4 -thio analog 15 of natural thymidine and the corresponding derivative of cytidine were prepared by Whistler and coworkers [11]. [Pg.401]

Potassium oxalate, 34, 83 Potassium permanganate, 30, 87 31,59 Potassium phthalimide, 38, 81 Potassium sulfide, 32,103 Potassium thiobenzoate, 32,101 Potassium thiocarbonate, 39, 78 Potassium thiocyanate, 32,39,40 Potassium trithiocarbonate, 39, 78 Prins reaction, 33, 72 Propane, 1, 3-dibromo-2,2-5m-(bromo-methyl)-, 31, 82... [Pg.55]

L-Arabinose diethyl dithioacetal was converted, via its 2,3-<9-isopropylidene derivative 298 and its thiobenzoate 299, into 4-azido-4-dco. y-5-lliio-a-D-xylopyranose triacetate (300).- " Ditosylation of 297, displacement of the 5-tosyloxy group by treatment with potassium thiobenzoate, and exchange of the 4-tosyloxy group with sodium azide in DMF gave the 5-az.ido-4-.S -benzoyl-D-xj lose derivative 301, isolated as the main compound (65%) via a 4,5-episulfonium intennediate. [Pg.58]

The first preparation of a chalcogenocarboxylato copper complex was described in the article by Engelhardt et al. [62] in 1868, who prepared thioben-zoic acid copper from the reaction of potassium thiobenzoate with CUSO4 in aqueous solution. The chemistry of this class of compounds, however, is not... [Pg.35]


See other pages where Potassium thiobenzoate is mentioned: [Pg.113]    [Pg.218]    [Pg.220]    [Pg.16]    [Pg.29]    [Pg.32]    [Pg.42]   
See also in sourсe #XX -- [ Pg.32 , Pg.101 ]

See also in sourсe #XX -- [ Pg.32 , Pg.101 ]

See also in sourсe #XX -- [ Pg.32 , Pg.101 ]

See also in sourсe #XX -- [ Pg.32 , Pg.101 ]

See also in sourсe #XX -- [ Pg.32 , Pg.101 ]

See also in sourсe #XX -- [ Pg.32 , Pg.101 ]

See also in sourсe #XX -- [ Pg.32 , Pg.101 ]

See also in sourсe #XX -- [ Pg.32 , Pg.101 ]

See also in sourсe #XX -- [ Pg.32 , Pg.101 ]

See also in sourсe #XX -- [ Pg.32 , Pg.101 ]

See also in sourсe #XX -- [ Pg.32 , Pg.101 ]

See also in sourсe #XX -- [ Pg.32 , Pg.101 ]




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Thiobenzoates

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