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That this process involves double inversion at C1 suggests the intermediacy of a tetramethylenechloronium ion. See
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34
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77951182566
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See the Supporting Information for the preparation of chloropolyols depicted in Table 1 and the stereochemical assignment of all compounds.
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See the Supporting Information for the preparation of chloropolyols depicted in Table 1 and the stereochemical assignment of all compounds.
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77951170183
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For selected examples, see
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For selected examples, see
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For selected examples of tetrahydrofuran formation via displacement of secondary alkyl chlorides see refs 7, 13b, and
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41
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77951169252
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2O provided oxepane (10%), 1,6-hexanediol (20%), and 7-oxa-1,13-tridecanediol (30%).
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2O provided oxepane (10%), 1,6-hexanediol (20%), and 7-oxa-1,13-tridecanediol (30%).
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77951193443
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See, for example
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Isolation of goniothalesdiol
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77951162168
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D +7.5 (c 0.23, EtOH)).
-
D +7.5 (c 0.23, EtOH)).
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