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- Takahashi Hironobu
- Institute of Pharmacognosy, Faculty of Pharmaceutical Sicences, Tokushima Bunri University
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- Tonoi Yasutoshi
- Institute of Pharmacognosy, Faculty of Pharmaceutical Sicences, Tokushima Bunri University
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- Matsumoto Keiji
- Institute of Pharmacognosy, Faculty of Pharmaceutical Sicences, Tokushima Bunri University
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- Minami Hiroyuki
- Institute of Pharmacognosy, Faculty of Pharmaceutical Sicences, Tokushima Bunri University
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- Fukuyama Yoshiyasu
- Institute of Pharmacognosy, Faculty of Pharmaceutical Sicences, Tokushima Bunri University
この論文をさがす
説明
The first synthesis of (−)-laurequinone, cyclolaurane-type sesquiterpenoid isolated from the red alga Laurencia nidifica, has been achieved by using an intramolecular Heck reaction and an insertion of carbene as the key steps for the construction of quaternary carbon at the benzylic position and cyclopropane ring, respectively.
収録刊行物
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- Chemistry Letters
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Chemistry Letters 27 (6), 485-486, 1998
公益社団法人 日本化学会
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詳細情報 詳細情報について
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- CRID
- 1390001204573600512
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- NII論文ID
- 130004421040
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- COI
- 1:CAS:528:DyaK1cXjs1OktL8%3D
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- ISSN
- 13480715
- 03667022
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- 本文言語コード
- en
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- データソース種別
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- JaLC
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- 使用不可