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- W2133358239 abstract "'Melo' out: A concise asymmetric synthesis of (−)-melotenine A has been accomplished in fourteen steps and 1 % overall yield from commercial N-tosylindole-3-carboxaldehyde. Key steps include a Piers annulation, an intermolecular vinylogous aldol reaction, and a novel one-pot sequence to prepare the ABCE tetracycle. Boc=tert-butoxycarbonyl, Ts=4-toluenesulfonyl. As a service to our authors and readers, this journal provides supporting information supplied by the authors. Such materials are peer reviewed and may be re-organized for online delivery, but are not copy-edited or typeset. Technical support issues arising from supporting information (other than missing files) should be addressed to the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article." @default.
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- W2133358239 date "2013-06-19" @default.
- W2133358239 modified "2023-10-17" @default.
- W2133358239 title "Total Synthesis of (−)-Melotenine A" @default.
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- W2133358239 doi "https://doi.org/10.1002/anie.201302517" @default.
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