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December 27, 2001Organic Letters

Total Synthesis of Spirotryprostatin B via Asymmetric Nitroolefination

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Abstract

[reaction: see text] A total synthesis of spirotryprostatin B was accomplished via asymmetric nitroolefination as a key step.

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Cite This Study

Bagul et al. (2001) studied this question.

synapsesocial.com/papers/6a787db8d2fa2470761f7b02 https://doi.org/10.1021/ol016999s

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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

1Palladium-catalyzed reactions in the synthesis of 3- and 4-substituted indoles. 2. Total synthesis of the N-acetyl methyl ester of (.+-.)-clavicipitic acidsOriginal Research · 1987 · 187 citations
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4The Asymmetric Total Synthesis of (+)- and (−)-Spirotryprostatin BOriginal Research · 2000 · 434 citations
5Enantioselective Creation of Quaternary Carbon Centers through Addition- Elimination Reaction: Asymmetric Nitroolefination of 3-Substituted 2-OxindolesOriginal Research · 1998 · 33 citations