The reaction of cycloalkanonhydrazones with mercaptoacetic acid. Synthesis of novel<i>N</i>-aminospirothiazolidinones
作者:R. Raji Reddy、D. S. Iyengar、U. T. Bhalerao
DOI:10.1002/jhet.5570220218
日期:1985.3
Cycloalkanone hydrazones undergo condensation with mercaptoacetic acid to give predominantly the spirothiazolidinones. The structures of the products have been established on the basis of physico-chemical data. These compounds have shown promising antibacterial and antifungal activity.
环烷酮hydr与巯基乙酸缩合,主要生成螺噻唑烷酮。产品的结构是根据理化数据确定的。这些化合物已显示出令人鼓舞的抗菌和抗真菌活性。