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   <subfield code="a">Synthesis of 2,6-diaminopyridine substituted α -oxoketene S , N -acetals: Crystal structure and hydrogen bonding interactions</subfield>
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   <subfield code="a">Polyaza α-oxoketene S,N-acetals can exist as either enamino or imino tautomeric forms. Based on the spectroscopic data and structural analysis of one of the S,N-acetals, the stereochemistry was unambiguously assigned as an all-E-configuration. The crystal structure confirms the enamino structure and shows extensive use of C-H⋯X (X = N, O, and S) weak hydrogen bonding interactions, thereby generating a 3-dimensional network in solid state. Graphical Abstract A new series of polyaza α-oxoketene S,N- acetals 3a-d was synthesized by thiomethyl displacement of α-oxoketene dithioacetals 2a-d with lithiated 2,6-diaminopyridine in good yields. The rotameric conformations and hydrogen bonding interactions are discussed with crystal structure.</subfield>
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