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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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 Creators:
Martin, Rene, Author
Dabritz, Frank, Author
Entchev, Eugeni V1, Author           
Kurzchalia, Teymuras V1, Author           
Knolker, Hans-Joachim, Author
Affiliations:
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: 2008
 Publication Status: Issued
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 Rev. Type: -
 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: -