BF3·OEt2 catalyzed [4 + 2] cycloaddition reactions of N-aryl Schiff's bases with 1-alkenyl, 1, 2-propadienyl, and 1-alkynyl sulfides

Koichi Narasaka; Takanori Shibata

doi:10.3987/COM-92-S(T)98

BF₃·OEt₂ catalyzed [4 + 2] cycloaddition reactions of N-aryl Schiff's bases with 1-alkenyl, 1, 2-propadienyl, and 1-alkynyl sulfides

Koichi Narasaka^*, Takanori Shibata

^*この研究の対応する著者

研究成果: Article › 査読

40 被引用数 (Scopus)

抄録

[4 + 2] Cycloaddition reaction proceeds between N-aryl Schiffs bases and 1-alkenyl sulfides, a 1, 2-propadienyl sulfide, or 1-alkynyl sulfides in the presence of BF₃·OEt₂ to provide 2-substituted quinoline derivatives. A 2-alkyl-4-quinolone alkaloid, leptomerine, is prepared by applying the present cycloaddition reaction.

本文言語	English
ページ（範囲）	1039-1053
ページ数	15
ジャーナル	Heterocycles
巻	35
号	2
DOI	https://doi.org/10.3987/COM-92-S(T)98
出版ステータス	Published - 1993 5月 1
外部発表	はい

ASJC Scopus subject areas

分析化学
薬理学
有機化学

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10.3987/COM-92-S(T)98

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「BF₃·OEt₂ catalyzed [4 + 2] cycloaddition reactions of N-aryl Schiff's bases with 1-alkenyl, 1, 2-propadienyl, and 1-alkynyl sulfides」の研究トピックを掘り下げます。これらがまとまってユニークなフィンガープリントを構成します。

引用スタイル

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abstract = "[4 + 2] Cycloaddition reaction proceeds between N-aryl Schiffs bases and 1-alkenyl sulfides, a 1, 2-propadienyl sulfide, or 1-alkynyl sulfides in the presence of BF3·OEt2 to provide 2-substituted quinoline derivatives. A 2-alkyl-4-quinolone alkaloid, leptomerine, is prepared by applying the present cycloaddition reaction.",

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doi = "10.3987/COM-92-S(T)98",

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N2 - [4 + 2] Cycloaddition reaction proceeds between N-aryl Schiffs bases and 1-alkenyl sulfides, a 1, 2-propadienyl sulfide, or 1-alkynyl sulfides in the presence of BF3·OEt2 to provide 2-substituted quinoline derivatives. A 2-alkyl-4-quinolone alkaloid, leptomerine, is prepared by applying the present cycloaddition reaction.

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