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.

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.

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Item Permalink: https://hdl.handle.net/21.11116/0000-000E-DF5C-1 Version Permalink: https://hdl.handle.net/21.11116/0000-000E-DF5D-0

Genre: Journal Article

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Creators:
Adam, W., Author
Güthlein, M., Author
Peters, E.-M.¹, Author
Peters, K.¹, Author
Wirth, T., Author

Affiliations:
1Former Scientific Facilities, Max Planck Institute for Solid State Research, Max Planck Society, ou_3370501

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Dates: Date issued: 1998

Publication Status: Issued

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Identifiers: eDoc: 182846
Other: 4237

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Title: Journal of the American Chemical Society

Source Genre: Journal

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Pages: - Volume / Issue: 120 Sequence Number: - Start / End Page: 4091 - 4093 Identifier: -