Photochemical rearrangements of 1-acetyl-1,2-dihydroquinoline-2-carbonitriles to the 3,1-benzoxazines and cycloprop[b]indoles

Masazumi Ikeda; Saeko Matsugashita; Chika Yukawa; Takayuki Yakura

doi:10.3987/COM-97-7978

Photochemical rearrangements of 1-acetyl-1,2-dihydroquinoline-2-carbonitriles to the 3,1-benzoxazines and cycloprop[b]indoles

Masazumi Ikeda^*, Saeko Matsugashita, Chika Yukawa, Takayuki Yakura

^*この論文の責任著者

分子合成化学研究室

研究成果: ジャーナルへの寄稿 › 学術論文 › 査読

6 被引用数 (Scopus)

抄録

Irradiation of 1-acetyl-1,2-dihydroquinoline-2-carbonitrile (1) in ether gave the 3,1-benzoxazine (3b), while the 4-methyl congener (2) in either ether or ethanol gave the 3,1-benzoxazine (4b) and the cycloprop[b]indole (7). A possible mechanism for the formation of these products is also discussed.

本文言語	英語
ページ（範囲）	121-126
ページ数	6
ジャーナル	Heterocycles
巻	49
号	1
DOI	https://doi.org/10.3987/COM-97-7978
出版ステータス	出版済み - 1998/12/31

ASJC Scopus 主題領域

分析化学
薬理学
有機化学

文献へのアクセス

10.3987/COM-97-7978

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引用スタイル

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abstract = "Irradiation of 1-acetyl-1,2-dihydroquinoline-2-carbonitrile (1) in ether gave the 3,1-benzoxazine (3b), while the 4-methyl congener (2) in either ether or ethanol gave the 3,1-benzoxazine (4b) and the cycloprop[b]indole (7). A possible mechanism for the formation of these products is also discussed.",

author = "Masazumi Ikeda and Saeko Matsugashita and Chika Yukawa and Takayuki Yakura",

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AU - Yukawa, Chika

AU - Yakura, Takayuki

PY - 1998/12/31

Y1 - 1998/12/31

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AB - Irradiation of 1-acetyl-1,2-dihydroquinoline-2-carbonitrile (1) in ether gave the 3,1-benzoxazine (3b), while the 4-methyl congener (2) in either ether or ethanol gave the 3,1-benzoxazine (4b) and the cycloprop[b]indole (7). A possible mechanism for the formation of these products is also discussed.

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