Approaches to the Cephalotaxine Skeleton Using an Intramolecular Heck Reaction.
書誌事項
- タイトル別名
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- Approaches to the Cephalotaxine Skeleto
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抄録
1-[2-(o-Iodophenyl)acetyl]-2-(prop-2-enyl)-2-vinylpyrrolidine (17), upon treatment with palladium(II) acetate [Pd(OAc)2] in the presence of triphenylphosphine and triethylamine in refluxing acetonitrile, gave the monocyclization product 20 as the major product along with a small amount of the tandem cyclization product 21. On the other hand, treatment of the 1-[2-(o-iodophenyl)acetyl]-1-azaspiro[4.4]non-8-en-7-one (25) with Pd(OAc)2, 1, 3-bis-(diphenylphosphino)propane, tributylphosphine, and silver carbonate in boiling N, N-dimethylformamide afforded the cyclized product 27 in 51% yield.
収録刊行物
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- CHEMICAL & PHARMACEUTICAL BULLETIN
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CHEMICAL & PHARMACEUTICAL BULLETIN 46 (7), 1084-1089, 1998
公益社団法人 日本薬学会
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詳細情報 詳細情報について
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- CRID
- 1390001204159222784
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- NII論文ID
- 130003773825
- 110003616983
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- NII書誌ID
- AA00602100
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- ISSN
- 13475223
- 00092363
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- NDL書誌ID
- 4538347
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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
- NDL
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- CiNii Articles
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- 抄録ライセンスフラグ
- 使用不可