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Stetter thiazolium salt method

For reviews, see Sielter Kuhlmann Org. React. 1991, 40, 407-496 Stetier Angew. Chem. Int. Ed. Engl. 1976, IS, 639-647 [Angew. Chem. 88, 695-704). For a similar method involving thiazolium salts, sec Stetter, Kuhlmann Chem, Her. 1976, 109, 2890 Stetter Skobel Chem. Ber. 1987, 120, 643 Stetter Kuhlmann Haese Org. Svruh. 65. [Pg.806]

Any of the d1 reagents suggested in chapter 25 would do but they preferred a catalytic method using the thiazolium salts 25 devised by Stetter.4 These are also aromatic heterocyclic compounds... [Pg.302]


See other pages where Stetter thiazolium salt method is mentioned: [Pg.1130]    [Pg.160]    [Pg.739]    [Pg.1133]    [Pg.432]    [Pg.191]    [Pg.161]   
See also in sourсe #XX -- [ Pg.6 , Pg.438 ]

See also in sourсe #XX -- [ Pg.6 , Pg.437 ]




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