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Synthesis of new 6-Spiro (Testosteron-3′-yl)-Hexahydro-3-Thioxo-1, 2, 3-Triazin-5-Ones and Related Derivatives as Affecting Enzymatic Agents

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A new 6-spiro (testosterone-3′-yl)-hexahydro-3-thioxo-1,2,3-triazin-5-ones (4a and 4b) have been synthesized by the condensation of testosterone and17-methyltestosterone(1a and 1b respectively) with thiosemicabazide. The first analogous 5 were obtained by oxidation while the second analogous 6-spiro (testosterone-3′-yl)-3-(4′-fluorophenyl)amino-1,2,3-triazin-5-ones (6) obtained by reaction of 4 with 4-fluoroaniline. These new compounds shows good to moderate affects on the activity of cellobiase produced by Aspergillus nidulans fungi.
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Keywords: Aspergillus nidulans; cellobiase; enzymatic agents; synthesis; testosterone-3; triazin

Document Type: Research Article

Publication date: June 1, 2015

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  • Current Organic Synthesis publishes in-depth reviews on all areas of synthetic organic chemistry i.e. asymmetric synthesis, organometallic chemistry, novel synthetic approaches to complex organic molecules, carbohydrates, polymers, protein chemistry, DNA chemistry, supramolecular chemistry, molecular recognition and new synthetic methods in organic chemistry. The frontier reviews provide the current state of knowledge in these fields and are written by experts who are internationally known for their eminent research contributions. The journal is essential reading to all synthetic organic chemists. Current Organic Synthesis should prove to be of great interest to synthetic chemists in academia and industry who wish to keep abreast with recent developments in key fields of organic synthesis.
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