The Chemistry of Indoles. XXIV. Syntheses of 3-Indoleacetic Acid and 3-Indoleacetonitrile Having a Halogeno Group and a Carbon Functional Group at the 4-Position

The Chemistry of Indoles. XXIV. Syntheses of 3-Indoleacetic Acid and 3-Indoleacetonitrile Having a Halogeno Group and a Carbon Functional Group at the 4-Position

フォーマット:

論文

責任表示:

Somei, Masanori ; Kizu, Kiyomi ; Kunimoto, Masako ; Yamada, Fumio

言語:

英語

出版情報:

Pharmaceutical Society of Japan = 日本薬学会, 1985-01-01

著者名:

掲載情報:

Chemical and Pharmaceutical Bulletin

ISSN:

0009-2363

巻:

33

通号:

9

開始ページ:

3696

終了ページ:

3708

バージョン:

publisher

概要:

Various 4-halogeno-3-indoleacetic acids and -3-indoleacetonitriles were synthesized for the first time by means of the Sandmeyer or Schiemann reaction, demonstrating the versatility of 4-indolediazonium salts in 4-substituted indole chemistry. A practical synthetic method for 4-halogenoindoles was developed by regio-selective thallation-halogenation, and the products were also led to 4-halogeno-3-indoleacetic acids. The first synthesis of … 4-formyl-3-indoleacetonitrile is also reported. 続きを見る

URL:

http://hdl.handle.net/2297/44021

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詳細

主題:	auxin
受理日:	1985-01-01

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4 論文 A novel preparation of 3-hydroxy-3H-indole-3-ethanamines and -3H-indole-3-acetamides having either a 4-morpholinyl or 1-pyrrolidinyl group at the 2-position Hayashi, Toshikatsu, Nakai, Yu-ya, Yamada, Fumio, Somei, Masanori 日本複素環化学研究所	10 論文 Three new synthetic methods for the 1,2,3,3a,8,8a-hexa-hydropyrrolo[2,3-b] indoles having an alkoxy group at the 3a-position Iwaki, Takako, Yamada, Fumio, Funaki, Shiho, Somei, Masanori 日本複素環化学研究所
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