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   <subfield code="a">Synthesis, Characterization and Structural Conformation Studies of 2-Amino-3-ethoxycarbonyl-4-(4′-methoxy Phenyl)-4H-pyrano-[3,2-c]-chromene-6-methyl-5-one</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[S. Naveen, S. Lakshmi, Dinesh Manvar, Alpesh Parecha, Anamik Shah, M. Sridhar, J. Shashidhara Prasad]</subfield>
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   <subfield code="a">2-amino-3-ethoxycarbonyl-4-(4′-methoxy Phenyl)-4H-pyrano-[3,2-c]-chromene-6-methyl-5-one was synthesized by the two-component reaction of 6-methyl-4-hydroxy coumarin with 4′-methoxy-2-cyano cinnamate, which was synthesized by Knoevenagel reaction with 88% yield. The compound obtained was characterized by spectroscopic techniques and confirmed by X-ray crystallographic studies. The crystallographic data analysis reveals that the title compound crystallizes in the triclinic space group $$P\overline{1}$$ with cell parameters a=7.7750(8)Å, b=9.0310(6)Å, c= 15.6120(17)Å, α=77.249(7)°, β= 115.860(3)°, γ=70.139(7)°, V=1,003.0(16)Å3 for Z=4. The structure has been solved by direct methods and refined to R1=0.0552 for 3,164 observed reflections with I&gt;2 σ(I). The pyran ring is in a flattened boat conformation. The carbonyl group is oriented in a -synperiplanar(cis) conformation.</subfield>
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