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- W2123669061 endingPage "1986" @default.
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- W2123669061 abstract "The total synthesis of the alkaloid (−)-chaetominine (1) has been achieved in four steps with an overall yield of 33.4%. Key features of our strategy include a one-pot cascade indole epoxidation – epoxide ring-opening cyclization – lactamization reaction sequence, and the use of a nitro group as a latent amino group for the one-pot construction of the quinazolinone ring. This constitutes a step economical, redox economical and protecting group-free total synthesis." @default.
- W2123669061 created "2016-06-24" @default.
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- W2123669061 date "2014-01-01" @default.
- W2123669061 modified "2023-10-07" @default.
- W2123669061 title "The four-step total synthesis of (−)-chaetominine" @default.
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- W2123669061 doi "https://doi.org/10.1039/c3cc48833k" @default.
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