Preparation of methyl 4,6-di-O-acetyl-3-
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Akinori Seta; Kiohisa Tokuda; Miki Kaiwa; Tohru Sakakibara
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Article
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1996
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Elsevier Science
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English
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The conformationally flexible title compounds were prepared and subjected to reduction with sodium borodeuteride. Deuteride ion attacks exclusively from the side opposite of the anomeric methoxyl group. However, the stereoselectivity of a similar reduction of the corresponding 4,6-O-benzylidene-~-I>