✦ LIBER ✦

ChemInform Abstract: The First Example of Oxiranyllithium and Oxiranyl Grignard Reagent Having a Carbanion Destabilizing Group: Generation, Property, and Some Synthetic Uses.

✍ Scribed by T. SATOH; K. HORIGUCHI

Book ID: 112027905
Publisher: John Wiley and Sons
Year: 2010
Weight: 32 KB
Volume: 27
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.199608111

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

The first example of oxiranyllithium and

The first example of oxiranyllithium and oxiranyl grignard reagent having a carbanion destabilizing group: Generation, property, and some synthetic uses

✍ Tsuyoshi Satoh; Kyoto Horiguchi 📂 Article 📅 1995 🏛 Elsevier Science 🌐 French ⚖ 243 KB

ChemInform Abstract: Generation of Oxira

ChemInform Abstract: Generation of Oxiranyllithiums and Oxiranyl Grignard Reagents Having a Carbanion-Destabilizing Group from Sulfinyloxiranes: Their Property and an Application to Asymmetric Synthesis of Epoxides and Alcohols.

✍ Tsuyoshi Satoh; Shigeko Kobayashi; Shino Nakanishi; Kyoko Horiguchi; Shiro Irisa 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 37 KB

Generation of oxiranyllithiums and oxira

Generation of oxiranyllithiums and oxiranyl Grignard reagents having a carbanion-destabilizing group from sulfinyloxiranes: Their property and an application to asymmetric synthesis of epoxides and alcohols

✍ Tsuyoshi Satoh; Shigeko Kobayashi; Shino Nakanishi; Kyoko Horiguchi; Shiro Irisa 📂 Article 📅 1999 🏛 Elsevier Science 🌐 French ⚖ 910 KB

The first generation of oxiranyllithiums and oxiranyl Grignard reagents having a carbanion-destabilizing group (alkyl group) was realized from sulfinyloxiranes via the ligand exchange reaction of sulfoxides with tert-butyllithium or ethylmagnesium chloridein THF at -80 to -100 \*C. The generated oxi