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- W2952006050 abstract "Abstract A new synthesis of the important aldehyde 1 from easily available 16-Dehydropregnenolone acetate (16-DPA) in high yield is described. The aldehyde 1 is converted to trio] 24, involving a stereoselective generation of all the four chiral centers in the brassinolide side chain. The important features of this synthesis is stereospecific generation of the acetate 14 through ene reaction using three different catalysts as well as regioselective wittig reaction on the acetoxy aldehyde 20. Conversion of triol 24 to brassinolide is known, hence this constitutes a formal total synthesis of brassinolide." @default.
- W2952006050 created "2019-06-27" @default.
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- W2952006050 date "2010-08-19" @default.
- W2952006050 modified "2023-09-26" @default.
- W2952006050 title "ChemInform Abstract: Stereoselective Synthesis of (22R,23R,24S)-3β-Hydroxy-5-ene-22,23- dihydroxy-24-methyl-cholestane: A Brassinolide Intermediate from 16- Dehydropregnenolone Acetate." @default.
- W2952006050 cites W2168553350 @default.
- W2952006050 doi "https://doi.org/10.1002/chin.199426231" @default.
- W2952006050 hasPublicationYear "2010" @default.
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