4.6 Article

I2/TBHP- Mediated tandem cyclization and oxidation reaction: Facile access to 2-substituted thiazoles and benzothiazoles

期刊

ORGANIC & BIOMOLECULAR CHEMISTRY
卷 17, 期 2, 页码 252-256

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ROYAL SOC CHEMISTRY
DOI: 10.1039/c8ob02826e

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资金

  1. National Natural Science Foundation of China [21602119, U1504208, 21702013]
  2. Beijing Natural Science Foundation [2184115]
  3. Fundamental Research Funds for the Central Universities [XK1802-6, buctrc201721]

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The efficient synthesis of 2-substituted thiazoles and benzothiazoles has been accomplished employing readily available cysteine esters and 2-aminobenzenethiols as N and S sources. The reaction proceeds under an I-2/TBHP system and involves a one-pot tandem cyclization and oxidation sequence. A diverse range of aldehydes is amenable for this transition-metal-free protocol, which provides an alternative method to rapidly access thiazole-containing molecules.

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