1,4-Cycloaddition reaction of enaminodithiocarboxylate derivatives with dimethyl acetylenedicarboxylate.
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説明
The reaction of enaminodithiocarboxylates, which have a conjugated thiocarbonyldiene system, with dimethyl acetylenedicarboxylate as a dienophile resulted in a 1, 4-cycloaddition to afford various thiapyrane derivatives and spiro (benzothiazoline) and thiazolinecyclopentadiene derivatives by the monodesulfurization. The reaction of thioamide derivatives of lepidine and 4-picoline gave benzoazocine and azocine derivatives.
収録刊行物
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- CHEMICAL & PHARMACEUTICAL BULLETIN
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CHEMICAL & PHARMACEUTICAL BULLETIN 23 (11), 2749-2758, 1975
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
- 1390001204168605056
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- NII論文ID
- 110003621765
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- NII書誌ID
- AA00602100
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- COI
- 1:CAS:528:DyaE28XnsVWlsw%3D%3D
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- ISSN
- 13475223
- 00092363
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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
- Crossref
- CiNii Articles
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- 抄録ライセンスフラグ
- 使用不可