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- W2039732564 abstract "Mansouramycin D, a cytotoxic alkaloid was isolated from a marine Streptomyces sp. in 2009. The first, simple, and concise route to the total synthesis of Mansouramycin D is reported. The core structure of the isoquinoline ring has been constructed from iminoannulation of 2-alkynylbenzaldehyde followed by oxidation/deprotection and oxidative amination via a three-step sequence from easily accessible starting materials." @default.
- W2039732564 created "2016-06-24" @default.
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- W2039732564 date "2013-12-09" @default.
- W2039732564 modified "2023-09-27" @default.
- W2039732564 title "Total Synthesis of the Marine Alkaloid Mansouramycin D" @default.
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- W2039732564 doi "https://doi.org/10.1021/ol4032396" @default.
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