✦ LIBER ✦

ChemInform Abstract: Development of Samarium Diiodide-Promoted Reductive Carbon—Nitrogen Bond Cleavage Reaction of α-Amino Carbonyl Compounds: Application to the Synthesis of Biologically Active Alkaloids

✍ Scribed by Toshio Honda

Publisher: John Wiley and Sons
Year: 2011
Weight: 20 KB
Volume: 42
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.201115248

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Development of Sama

ChemInform Abstract: Development of Samarium Diiodide Promoted Regioselective Carbon—Carbon Bond Cleavage Reaction of γ-Halo- and ε-Halo-α,β-Unsaturated Carbonyl Compounds: Application to the Synthesis of Biologically Active Natural Products

✍ Toshio Honda 📂 Article 📅 2011 🏛 John Wiley and Sons ⚖ 20 KB 👁 1 views

ChemInform Abstract: Application of Sama

ChemInform Abstract: Application of Samarium Diiodide-Promoted Reductive Carbon—Nitrogen Bond Cleavage Reaction to 3-Oxopyrrolidine Derivatives: Alternative Synthesis of a Coccinellid Alkaloid, (-)-Adalinine.

✍ Toshio Honda; Chihiro Hisa 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 23 KB 👁 1 views

## Abstract The application of the samarium diiodide fragmentation reaction to 5,5‐disubstituted oxopyrrolidines (I) leads to a regioselective carbon—nitrogen bond cleavage affording the 4,4‐disubstituted cleavage products (II).