Stereoselective synthesis of the hormonally active (25S)-delta7-dafachronic 
acid, (25S)-Delta4-dafachronic acid, (25S)-dafachronic acid, and 
(25S)-cholestenoic acid

Martin, Rene; Dabritz, Frank; Entchev, Eugeni V; Kurzchalia, Teymuras V; Knolker, Hans-Joachim

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Stereoselective synthesis of the hormonally active (25S)-delta7-dafachronic acid, (25S)-Delta4-dafachronic acid, (25S)-dafachronic acid, and (25S)-cholestenoic acid

Martin, R., Dabritz, F., Entchev, E. V., Kurzchalia, T. V., & Knolker, H.-J. (2008). Stereoselective synthesis of the hormonally active (25S)-delta7-dafachronic acid, (25S)-Delta4-dafachronic acid, (25S)-dafachronic acid, and (25S)-cholestenoic acid. Organic & Biomolecular Chemistry, 6(23), 4293-4295.

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Item Permalink: https://hdl.handle.net/21.11116/0000-0001-0EA0-B Version Permalink: https://hdl.handle.net/21.11116/0000-0001-0EA1-A

Genre: Journal Article

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Creators:
Martin, Rene, Author
Dabritz, Frank, Author
Entchev, Eugeni V¹, Author
Kurzchalia, Teymuras V¹, Author
Knolker, Hans-Joachim, Author

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1Max Planck Institute of Molecular Cell Biology and Genetics, Max Planck Society, ou_2340692

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Abstract: We report a stereoselective synthesis of the (25S)-cholestenoic-26-acids which are highly efficient ligands for the hormonal receptor DAF-12 in Caenorhabditis elegans.

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Dates: Date issued: 2008

Publication Status: Issued

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Identifiers: eDoc: 414344
Other: 1135

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Title: Organic & Biomolecular Chemistry

Source Genre: Journal

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Pages: - Volume / Issue: 6 (23) Sequence Number: - Start / End Page: 4293 - 4295 Identifier: -