References
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Tet. Lett.
We originally reported that photolysis of A gave small amounts of compound B resulting from [3+2] cycloaddition of the side chain olefin with an intermediate thiocarbonyl ylide. This assignment was made on the basis of ¹H and
$^13$ C NMR data. The correct structure C, however, was later determined by single crystal X-ray analysis Dittami,J.P.(et al.) - Acc. Chem. Res. v.15 For recent reviews of [2+2] cycloaddition reactions see;Intramolecular [2+2] Photoaddition/Cyclobutane-Fragmentation Sequence in Orgainc Synthesis Oppolzer,W.
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Photoaddition of S₁ Naphthalene to S
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