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First Example of a Highly Enantioselective Catalytic Protonation of Silyl Enol Ethers Using a Novel Lewis Acid-Assisted Brønsted Acid System

✍ Scribed by Ishihara, Kazuaki; Nakamura, Shingo; Kaneeda, Masanobu; Yamamoto, Hisashi

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: First Example of a

✍ K. ISHIHARA; S. NAKAMURA; M. KANEEDA; H. YAMAMOTO 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB 👁 2 views

The Crystallographic Structure of a Lewi

✍ Ishihara, Kazuaki; Nakashima, Daisuke; Hiraiwa, Yukihiro; Yamamoto, Hisashi 📂 Article 📅 2003 🏛 American Chemical Society 🌐 English ⚖ 67 KB

Enantioselective Protonation of Silyl En

✍ Nakamura, Shingo; Kaneeda, Masanobu; Ishihara, Kazuaki; Yamamoto, Hisashi 📂 Article 📅 2000 🏛 American Chemical Society 🌐 English ⚖ 291 KB

Lewis Acid Assisted Chiral Bronsted Acid

✍ Ishihara, Kazuaki; Kaneeda, Masanobu; Yamamoto, Hisashi 📂 Article 📅 1994 🏛 American Chemical Society 🌐 English ⚖ 321 KB

The Crystallographic Structure of a Lewi

✍ Kazuaki Ishihara; Daisuke Nakashima; Yukihiro Hiraiwa; Hisashi Yamamoto 📂 Article 📅 2003 🏛 John Wiley and Sons ⚖ 174 KB 👁 2 views

ChemInform Abstract: Chiral Broensted Ac

✍ Cheol Hong Cheon; Osamu Kanno; F. Dean Toste 📂 Article 📅 2011 🏛 John Wiley and Sons ⚖ 57 KB 👁 1 views

## Abstract Optically active cyclohexanones as well as a cycloheptanone are formed from the corresponding silyl enol ethers.