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Stereoselective synthesis of d-erythro- and l-threo-sphinganines via palladium-catalyzed equilibration and Suzuki coupling

✍ Scribed by Gregory R. Cook; Ketheeswaran Pararajasingham


Publisher
Elsevier Science
Year
2002
Tongue
French
Weight
209 KB
Volume
43
Category
Article
ISSN
0040-4039

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✦ Synopsis


The Pd-catalyzed isomerization of 5-vinyloxazolines was utilized for the stereoselective synthesis of D-erythro -and L-threo -spinganine triacetate. A hydroboration/Suzuki coupling sequence was employed to elongate the hydrophobic chain.


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