scholarly journals Synthesis of 3-Ferrocenyl Isocoumarins

2020 ◽  
Vol 36 (05) ◽  
pp. 976-979
Author(s):  
Neeta Sinha

The derivatives of 3-ferrocenyl isocoumarin were synthesized by the condensation of substituted homothphalic anhydride with ferrocene using phosphoric acid or anhydrous aluminium chloride as cyclising agent. Substituted homophthalic acid did not condense with ferrocene so homophthalic acids were converted into their anhydride and then allowed to react with ferrocene in the presence of polyphosphoric acid or in the presence of anhydrous aluminium chloride using dichloromethane as the solvent to give 3-ferrocenyl isocoumarins. 7-Methoxy, 6-methyl, 5,7-dihydroxy, 6,7-dimethoxy and 5,7-dimethoxy derivatives of 3-ferrocenyl isocoumarin were synthesized. All the compounds were characterised by melting point determination, elemental and spectral analysis.

1993 ◽  
Vol 12 (22) ◽  
pp. 1733-1734 ◽  
Author(s):  
S. Ahila ◽  
S. Ramakrishna Iyer ◽  
V. M. Radhakrishnan

1965 ◽  
Vol 49 (1) ◽  
pp. 97-106 ◽  
Author(s):  
S. Sulimovici ◽  
B. Lunenfeld ◽  
M. C. Shelesnyak

ABSTRACT A method is described for the assay of urinary pregnanediol and allopregnanediol which employs acid hydrolysis of pregnanediol glucuronide, ascending thin-layer chromatography and spectrophotometric quantitation of the eluted pregnanediol and allopregnanediol. The reliability of the method was established by analysis of infra-red and UV absorption spectra, melting point determination, recovery experiments, duplicate assays and comparison with the Klopper method. The method has advantages in that it is rapid and requires small urine samples.


1972 ◽  
Vol 18 (1) ◽  
pp. 45-49 ◽  
Author(s):  
A. J. Cserjesi ◽  
E. L. Johnson

The formation of pentachloroanisole by methylation from pentachlorophenol by Trichoderma virgatum in liquid cultures was detected using gas chromatography and confirmed by melting point determination and infrared (i.r.) spectroscopy. The formation of pentachloroanisole, however, did not account for the total loss of pentachlorophenol in the medium, suggesting that this reaction is only the first step in the metabolism of this compound or a parallel reaction to degradation. Pentachloroanisole was much less toxic than pentachlorophenol to Trichoderma virgatum, Cephaloascus fragrans, and Penicillium sp., as well as to fish in laboratory toxicity tests.


Sign in / Sign up

Export Citation Format

Share Document