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Heck-Type Cyclization of Oxime Ethers: Stereoselective Carbon–Carbon Bond Formation with Aryl Halides To Produce Heterocyclic Oximes

✍ Scribed by Hiroaki Ohno; Akimasa Aso; Yoichi Kadoh; Nobutaka Fujii; Tetsuaki Tanaka

Publisher: John Wiley and Sons
Year: 2007
Tongue: English
Weight: 122 KB
Volume: 46
Category: Article
ISSN: 0044-8249
DOI: 10.1002/anie.200701868

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✦ Synopsis

Scheme 1. Cyclization of the allenic oxime ether 1, and a plausible mechanism. Mts = 2,4,6-trimethylphenylsulfonyl.

📜 SIMILAR VOLUMES

Heck-Type Cyclization of Oxime Ethers: S

Heck-Type Cyclization of Oxime Ethers: Stereoselective Carbon—Carbon Bond Formation with Aryl Halides to Produce Heterocyclic Oximes.

✍ Hiroaki Ohno; Akimasa Aso; Yoichi Kadoh; Nobutaka Fujii; Tetsuaki Tanaka 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 35 KB

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