Concise Synthesis of the Antiplasmodial Isocyanoterpene 7,20‐Diisocyanoadociane

The flagship member of the antiplasmodial isocyanoterpenes, 7,20‐diisocyanoadociane (DICA), was synthesized from dehydrocryptone in 10 steps, and in 13 steps from commercially available material. Our previous formal synthesis was reengineered, leveraging only productive transformations to deliver DI...

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Vydáno v:Angewandte Chemie International Edition Ročník 58; číslo 39; s. 13749 - 13752
Hlavní autoři: Karns, Alexander S., Ellis, Bryan D., Roosen, Philipp C., Chahine, Zeinab, Le Roch, Karine G., Vanderwal, Christopher D.
Médium: Journal Article
Jazyk:angličtina
Vydáno: WEINHEIM Wiley 23.09.2019
Wiley Subscription Services, Inc
Vydání:International ed. in English
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ISSN:1433-7851, 1521-3773, 1521-3773
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Shrnutí:The flagship member of the antiplasmodial isocyanoterpenes, 7,20‐diisocyanoadociane (DICA), was synthesized from dehydrocryptone in 10 steps, and in 13 steps from commercially available material. Our previous formal synthesis was reengineered, leveraging only productive transformations to deliver DICA in fewer than half the number of steps of our original effort. Important contributions, in addition to the particularly concise strategy, include a solution to the problem of axial nucleophilic methylation of a late‐stage cyclohexanone, and the first selective synthesis and antiplasmodial evaluation of the DICA stereoisomer with both isonitriles equatorial. The flagship antiplasmodial isocyanoterpene, 7,20‐diisocyanoadociane (DICA), was constructed in ten steps from simple starting materials. An additional important contribution is a solution to the problem of axial nucleophilic methylation of a late‐stage cyclohexanone, and the first selective synthesis and antiplasmodial evaluation of the DICA stereoisomer with both isonitriles equatorial.
Bibliografie:These authors contriuted equally to this work.
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These authors contributed equally.
ISSN:1433-7851
1521-3773
1521-3773
DOI:10.1002/anie.201906834