𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis of 2-Oxozolidinones from β-Lactams: Stereospecific Total Synthesis of (-)-Cytoxazone and All of Its Stereoisomers.

✍ Scribed by Rajesh Kumar Mishra; Cristina M. Coates; Kevin D. Revell; Edward Turos

Publisher
John Wiley and Sons
Year
2007
Weight
13 KB
Volume
38
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

The stereospecific synthesis of all four
The stereospecific synthesis of all four stereoisomers of 2-amino-6-phenoxy-cyclohexanol,
✍ Edouard Lier; Richard Berthold; Franz Troxler 📂 Article 📅 1979 🏛 John Wiley and Sons 🌐 German ⚖ 534 KB

## Abstract Epoxidation of 3‐phenoxycyclohexene **5** with __m__‐chloro‐perbenzoic acid gave **6** and **7** in a ratio of 9:1. These two epoxides were heated with a series of amines to give the aminophenoxycyclohexanol derivatives **1** and **2** respectively; in all cases the reaction was regio‐

Stereospecific Benzyne-Induced Olefinati
Stereospecific Benzyne-Induced Olefination from β-Amino Alcohols and Its Application to the Total Synthesis of (−)-1-Deoxy-D-fructose
✍ Prof. Jih Ru Hwu; Dr. Yung Chang Hsu 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 249 KB 👁 1 views

Chemists endeavor to develop efficient methods for the generation of carbon-carbon double bonds in organic and biomolecules with stereospecificity. [1] The outcomes benefit synthetic and natural product chemistry to a great extent. Herein, we contribute a new method to form the C=C bond that is comp