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   <subfield code="a">Oxidative opening of the 2,5-dihydroxy-3,4,6,7-tetrachlorocoumaran ring</subfield>
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   <subfield code="c">[G. Karlivan, V. Zin'kovskaya, R. Valter, R. Kampare]</subfield>
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   <subfield code="a">A method has been developed for the synthesis of (3,5,6-trichloro-1,4-benzoquinone-2-yl)chloroacetaldehyde by the oxidative ring opening of 2,5-dihydroxy-3,4,6,7-tetrachlorocoumaran with nitrogen oxides. The ion-radical salt of (3,5,6-trichloro-1,4-benzoquinone-2-yl)chloroacetaldehyde with N,N,N′,N′-tetramethyl-p-phenylenediamine (1∶1) has been synthesized. The reaction of 2,5-dihydroxy-3,4,6,7-tetrachlorocoumaran-3-yl) with pyridine gave N-(2,5-dihydroxy-4,6,7-trichlorocoumaran-3-yl)pyridine chloride, which is also formed from the opening of the coumaran ring.</subfield>
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