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An Efficient and Straightforward Access to Sulfur Substituted [2.2]Paracyclophanes: Application to Stereoselective Sulfenate Salt Alkylation
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A straightforward and high-yielding access to various [2.2]paracyclophanes possessing a sulfur-based functional group is reported, the keystep being a SEAr reaction mediated by a sulfonium salt. The versatility of the methodology was exemplified by an original application insulfenate salt chemistry, from which a remarkable chirality transfer was observed.

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