In the present paper, we report an expedient total synthesis of triciribine, a tricyclic 7-deazapurine nucleoside and protein kinase B (AKT ) inhibitor, in 35% overall yield. Our synthesis route features a highly regioselective substitution of 1--Boc-2-methylhydrazine and a trifluoroacetic acid catalyzed one-pot transformation which combined the deprotection of the -butylcarbonyl (Boc) group and ring closure reaction together to give a tricyclic nucleobase motif.
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| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6154533 | PMC |
| http://dx.doi.org/10.3390/molecules22040643 | DOI Listing |
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