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https://doi.org/10.1002/chin.199229272
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Cite Journal: ChemInform |  Publication Date: Aug 21, 2010 |
Ynamines 1a–d are prepared by alkylation of nucleic acids bases with tetrachloroethylene followed by elimination of halogens from the intermediates 4a–d; reaction of 1a with acetone and cyclohexanone gives carbinols 8a and b and in the case of 8b cyclic ketal 9a is also obtained; compound 1a is a substrate for adenosine deaminase.
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