Chiral-auxiliary-induced diastereoselectivity in the [4 + 2] cycloadditions of 
optically active 2,2-dimethyloxazolidine derivatives of sorbic acid: a model 
study with singlet oxygen as the smallest dienophile.

Adam, W.; Güthlein, M.; Peters, E.-M.; Peters, K.; Wirth, T.

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Chiral-auxiliary-induced diastereoselectivity in the [4 + 2] cycloadditions of optically active 2,2-dimethyloxazolidine derivatives of sorbic acid: a model study with singlet oxygen as the smallest dienophile.

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Peters, E.-M.
Former Scientific Facilities, Max Planck Institute for Solid State Research, Max Planck Society;

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Peters, K.
Former Scientific Facilities, Max Planck Institute for Solid State Research, Max Planck Society;

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Adam, W., Güthlein, M., Peters, E.-M., Peters, K., & Wirth, T. (1998). Chiral-auxiliary-induced diastereoselectivity in the [4 + 2] cycloadditions of optically active 2,2-dimethyloxazolidine derivatives of sorbic acid: a model study with singlet oxygen as the smallest dienophile. Journal of the American Chemical Society, 120, 4091-4093.

Cite as: https://hdl.handle.net/21.11116/0000-000E-DF5C-1

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