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note
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-3; 1379 independent reflections; R = 0.0720. Further details of the crystal structure of sesquioxide 5 are available on request from the Cambridge Crystallographic Data Centre by quoting the names of the authors and the journal citation.
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41
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0025259615
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and references cited therein
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Since the nomenclature for the stereochemical prefixes of unsymetrically substituted brigde atoms is far from being unique, we prefer, with regard to earlier communications concerning Diels-Alder reactions of thiophene S-oxides, to name the configuration of the sulfoxide group syn when the oxygen atom directs toward the second ring and anti when it directs away from it. For a more detailed discussion, see: Macauley, J. B.; Fallis, A. G. J. Am. Chem. Soc. 1990, 112, 1136-1144 and references cited therein.
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note
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-3; 1291 independent reflections; R = 0.0433. Further details of the crystal structure of dimer 4a are available on request from the Cambridge Crystallographic Data Centre by quoting the names of the authors and the journal citation.
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