Diastereoselective and regioselective singlet-oxygen ene reaction of 
oxazolidine-substituted alkenes: Control through hydrogen bonding mediated by 
the urea functionality of chiral auxiliaries

Adam, W.; Peters, K.; Peters, E.-M.; Schambony, S. B.

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Diastereoselective and regioselective singlet-oxygen ene reaction of oxazolidine-substituted alkenes: Control through hydrogen bonding mediated by the urea functionality of chiral auxiliaries

Adam, W., Peters, K., Peters, E.-M., & Schambony, S. B. (2000). Diastereoselective and regioselective singlet-oxygen ene reaction of oxazolidine-substituted alkenes: Control through hydrogen bonding mediated by the urea functionality of chiral auxiliaries. Journal of the American Chemical Society, 122, 7610-7611.

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Item Permalink: https://hdl.handle.net/21.11116/0000-000E-EDC7-7 Version Permalink: https://hdl.handle.net/21.11116/0000-000E-EDC8-6

Genre: Journal Article

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Creators:
Adam, W., Author
Peters, K.¹, Author
Peters, E.-M.¹, Author
Schambony, S. B., Author

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

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Dates: Date issued: 2000

Publication Status: Issued

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Identifiers: eDoc: 181278
Other: 26866

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Title: Journal of the American Chemical Society

Source Genre: Journal

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Pages: - Volume / Issue: 122 Sequence Number: - Start / End Page: 7610 - 7611 Identifier: -