A short and efficient synthesis of (2S,3S,4S)-tert-butyl 3,4-dihydroxy-2-(methoxymethyl)-5-oxopyrrolidine-1-carboxylate
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A1 Alkuperäisartikkeli tieteellisessä aikakauslehdessä
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Date
2010
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Language
en
Pages
2816-2822
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SYNTHESIS: STUTTGART, issue 16
Abstract
Asymmetric synthesis of the title compound was accomplished starting from L-serine. Stannoxane-mediated lactamization provided the key intermediate in good yield.Description
Keywords
natural products, stereoselective synthesis, olefination, alpha,beta-unsaturated lactam, dihydroxylation
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Citation
Passiniemi , M & Koskinen , A M P 2010 , ' A short and efficient synthesis of (2S,3S,4S)-tert-butyl 3,4-dihydroxy-2-(methoxymethyl)-5-oxopyrrolidine-1-carboxylate ' , SYNTHESIS: STUTTGART , no. 16 , pp. 2816-2822 . https://doi.org/10.1055/s-0029-1218843