Enantioselective Intramolecular C鈥揌 Insertion Reactions of Donor鈥揇onor Metal Carbenoids
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文摘
The first asymmetric insertion reactions of donor鈥揹onor carbenoids, i.e., those with no pendant electron-withdrawing groups, are reported. This process enables the synthesis of densely substituted benzodihydrofurans with high levels of enantio- and diastereoselectivity. Preliminary results show similar efficiency in the preparation of indanes. This new method is used in the first enantioselective synthesis of an oligoresveratrol natural product (E-未-viniferin).

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