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Catalytic, Highly Enantio, and Diastereoselective Nitroso Diels−Alder Reaction

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NIAID Data Ecosystem2026-03-06 收录
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This communication presents studies that nitroso Diels−Alder adduct has been furnished in uniformly high yield and high enantioselectivity using nitrosopyridine as a substrate and copper as a catalyst. The obtained Diels−Alder adduct was easily transformed to corresponding chiral amino alcohols without loss of enantioselectivity.

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2016-05-07
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