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• W2952319742 abstract "1-Deoxy-d-galactohomonojirimycin was synthesized in seven steps from optically pure allenylstannane 4 and l-lactate-derived aldehyde 5 in 48% overall yield. The key step was the Lewis acid catalyzed reaction of 4 and 5 to give the syn-amino alcohol in excellent yield and very high diastereoselectivity." @default.
• W2952319742 created "2019-06-27" @default.
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• W2952319742 date "2003-12-12" @default.
• W2952319742 modified "2023-10-16" @default.
• W2952319742 title "Synthesis of 1-Deoxy-<scp>d</scp>-galactohomonojirimycin via Enantiomerically Pure Allenylstannanes" @default.
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• W2952319742 doi "https://doi.org/10.1021/jo0303012" @default.
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