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   <subfield code="a">Ultrasonic synthesis and crystal structure analysis of two trimethylsilyloxy-substituted bicyclo[2.2.2]octene derivatives</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[H SRINIVASA, H NAGARAJAIAH, B PALAKSHAMURTHY, S HARIPRASAD, NOOR BEGUM]</subfield>
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   <subfield code="a">The compounds: 11-trimethylsilyloxy-1,2,3,4,4a,9a-hexahydro-1,4-etheno-anthraquinone and 4-benzyl-8-trimethylsilyloxy-4-aza-tricyclo[5.2.2.0]undec-8-ene-3,5-dione were synthesized by the Diels-Alder [4 π s  + 2 π s ] cycloaddition reaction of 2-(trimethylsilyloxy)-1,3-cyclohexadiene with naphthaquinone and N-benzylmaleimide under ultrasonic conditions. The crystal structure analysis was done using single crystal X-ray diffraction method. In both the compounds, the trimethylsilyloxy- and naphthaquinone/ N-benzylmaleimide moieties are endo- to the bicyclic ring. Graphical Abstract The synthesis of two novel trimethylsilyloxy- substituted bicyclo[2.2.2]octene derivatives by employing ultrasonic reaction conditions is reported. The compounds have been characterized by single crystal X-ray studies.</subfield>
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