Tandem Migration-Carboalkoxylation of o-Isocyanophenyl Acetals Leading to Benzoxazoles

Takashi Okitsu; Kenta Nagase; Nobuhiko Nishio; Akimori Wada

doi:10.1021/ol203175a

Tandem Migration-Carboalkoxylation of o-Isocyanophenyl Acetals Leading to Benzoxazoles

Takashi Okitsu, Kenta Nagase, Nobuhiko Nishio, Akimori Wada^*

^*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

23 被引用数 (Scopus)

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An efficient approach to benzoxazoles via tandem migration - carboalkoxylation of o-isocyanophenyl acetals has been developed. Both a Lewis acid and base are essential for this reaction, and the BF ₃· OEt ₂/2,4,6-collidine combination is the best choice for cooperative transformation.

本文言語	英語
ページ（範囲）	708-711
ページ数	4
ジャーナル	Organic Letters
巻	14
号	3
DOI	https://doi.org/10.1021/ol203175a
出版ステータス	出版済み - 2012/02/03

ASJC Scopus 主題領域

生化学
物理化学および理論化学
有機化学

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10.1021/ol203175a

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abstract = "An efficient approach to benzoxazoles via tandem migration - carboalkoxylation of o-isocyanophenyl acetals has been developed. Both a Lewis acid and base are essential for this reaction, and the BF 3· OEt 2/2,4,6-collidine combination is the best choice for cooperative transformation.",

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AU - Wada, Akimori

PY - 2012/2/3

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AB - An efficient approach to benzoxazoles via tandem migration - carboalkoxylation of o-isocyanophenyl acetals has been developed. Both a Lewis acid and base are essential for this reaction, and the BF 3· OEt 2/2,4,6-collidine combination is the best choice for cooperative transformation.

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Tandem Migration-Carboalkoxylation of o-Isocyanophenyl Acetals Leading to Benzoxazoles

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