## A stereocontrolled synthesis of Cl6 Summary: -PAF ( 11) from (S)-(-)-malic acid (I), employing regioselective hydrogenolytic cleavage of benzyEdene acetal derivatives of (S)-I,2,4butanetriol (1) with borane-tetrahydrofran complex, is described. 1-0-A1kyl-2-0-acetyl-sn-glyceryl-3-phosphorylcholi
An efficient and stereoselective synthesis of platelet-activating factors and the enantiomers from D- and L- tartaric acids
β Scribed by Kagari Fujita; Hisao Nakai; Susumu Kobayashi; Keizo Inoue; Shoshichi Nojima; Masaji Ohno
- Publisher
- Elsevier Science
- Year
- 1982
- Tongue
- French
- Weight
- 246 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
Acetyl glyceryl ether phosphorylcholines, platelet-activating factors (1 and 21, were efficiently synthesized in a stereochemically unambiguous manner starting from D-and L-tartaric acids as the chiral synthons.
Since its isolation and characterization by Hanahan and his co-workers in
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