Total Synthesis of Lyconesidine B, a Lycopodium Alkaloid with an Oxygenated, Amine-Type Fawcettimine Core
抄録
This report describes the total synthesis of the complex, oxygenated tetracyclic alkaloid, lyconesidine B. The key synthetic challenge involves diastereoselective generation of a decahydroquinoline ring with a quaternary carbon at the angular position via domino cyclopropanation, ring-opening, and reduction. Another crucial step is the domino ene-yne metathesis involving a quaternary ammonium ion, leading to the construction of a decahydroazaazulen framework.
収録刊行物
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- Organic Letters
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Organic Letters 23 (3), 676-681, 2021-02
American Chemical Society (ACS)
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詳細情報 詳細情報について
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- CRID
- 1050571948037518720
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- NII論文ID
- 120007177779
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- ISSN
- 15237052
- 15237060
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- HANDLE
- 2433/266607
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- 本文言語コード
- en
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- 資料種別
- journal article
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- データソース種別
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- IRDB
- CiNii Articles