Synthesis of the enantiomeric 1,4,5,6-te
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Karol S. Bruzik; Grzegorz M. SalamoΕczyk
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Article
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1989
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Elsevier Science
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English
β 490 KB
The synthesis of the optically pure 1,4,5,6-tetra-O-benzyl-myo-inositols was achieved in four steps via diastereomeric 2,3-spire-acetals of myo-inositol with Land D-camphor as the key intermediates. Camphor dimethyl acetal was used for the acetalation reaction. The diastereomers were benzylated and