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Benzthiazole-2-thiol

In a further exanple. Smith and Wan exploited the nucleophilic capability of l-phenyl-2-tetrazoline-5-thione in the Mitsunobu reaction, followed by oxidation to the sulfone with hydrogen peroxide and ammonium heptamolybdate tetrahydrate as a key step in a synthesis of the ansamycin antiobiotic, (+ )-thiazinotrienomycin-E (eq 8). Importantly, use of the phenyltetrazolylthione-derived sulfone gave an 13Z ratio of 10 1 in this coupling whereas the more conventional benzthiazole-2-thiol-derived system resulted in a selectivity of only 1.5 1 in favor of the -isomer. [Pg.455]

Related Reagents. Benzthiazole-2-thiol l-terf-Butyl-l//-2-tetrazoline-5-thione. [Pg.456]

The 9-heteroarylthiomethyl derivative 70 was prepared by a comparable process utilizing silver nitrate to catalyze the reaction between carbazole, formaldehyde, and the benzthiazole thiol. °... [Pg.110]

Cul/Bipy-Mediated Direct Sulfurization of Benzthiazoles with Thiols... [Pg.212]




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