Smooth isoindolinone formation from isopropyl carbamates via bischler-napieralski-type cyclization

Satoshi Adachi; Masao Onozuka; Yuko Yoshida; Mitsuaki Ide; Yoko Saikawa; Masaya Nakata

doi:10.1021/ol403142d

Smooth isoindolinone formation from isopropyl carbamates via bischler-napieralski-type cyclization

Satoshi Adachi, Masao Onozuka, Yuko Yoshida, Mitsuaki Ide, Yoko Saikawa, Masaya Nakata

応用化学科

研究成果: Article › 査読

51 被引用数 (Scopus)

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Isopropyl carbamates derived from benzylamines provide isoindolinones by treatment with phosphorus pentoxide at room temperature. Utility of this Bischler-Napieralski-type cyclization and a new mechanism involving a carbamoyl cation for rationalization of this smooth conversion are discussed.

本文言語	English
ページ（範囲）	358-361
ページ数	4
ジャーナル	Organic Letters
巻	16
号	2
DOI	https://doi.org/10.1021/ol403142d
出版ステータス	Published - 2014 3月 17

ASJC Scopus subject areas

生化学
物理化学および理論化学
有機化学

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10.1021/ol403142d

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title = "Smooth isoindolinone formation from isopropyl carbamates via bischler-napieralski-type cyclization",

abstract = "Isopropyl carbamates derived from benzylamines provide isoindolinones by treatment with phosphorus pentoxide at room temperature. Utility of this Bischler-Napieralski-type cyclization and a new mechanism involving a carbamoyl cation for rationalization of this smooth conversion are discussed.",

author = "Satoshi Adachi and Masao Onozuka and Yuko Yoshida and Mitsuaki Ide and Yoko Saikawa and Masaya Nakata",

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T1 - Smooth isoindolinone formation from isopropyl carbamates via bischler-napieralski-type cyclization

AU - Adachi, Satoshi

AU - Onozuka, Masao

AU - Yoshida, Yuko

AU - Ide, Mitsuaki

AU - Saikawa, Yoko

AU - Nakata, Masaya

PY - 2014/3/17

Y1 - 2014/3/17

N2 - Isopropyl carbamates derived from benzylamines provide isoindolinones by treatment with phosphorus pentoxide at room temperature. Utility of this Bischler-Napieralski-type cyclization and a new mechanism involving a carbamoyl cation for rationalization of this smooth conversion are discussed.

AB - Isopropyl carbamates derived from benzylamines provide isoindolinones by treatment with phosphorus pentoxide at room temperature. Utility of this Bischler-Napieralski-type cyclization and a new mechanism involving a carbamoyl cation for rationalization of this smooth conversion are discussed.

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Smooth isoindolinone formation from isopropyl carbamates via bischler-napieralski-type cyclization

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