✦ LIBER ✦

Studies Directed toward the Total Synthesis of Cerorubenic Acid-III. 5. A Radical Cyclization Route Leading to the Methyl Ester of the Natural Isomer 1

✍ Scribed by Paquette, Leo A.; Dyck, Brian P.

Book ID: 127128587
Publisher: American Chemical Society
Year: 1998
Tongue: English
Weight: 215 KB
Volume: 120
Category: Article
ISSN: 0002-7863
DOI: 10.1021/ja980691n

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Studies Directed To

ChemInform Abstract: Studies Directed Toward the Total Synthesis of Cerorubenic Acid-III. Part 5. A Radical Cyclization Route Leading to the Methyl Ester of the Natural Isomer.

✍ L. A. PAQUETTE; B. P. DYCK 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 45 KB 👁 2 views

ChemInform Abstract: Model Studies Direc

ChemInform Abstract: Model Studies Directed Toward the Total Synthesis of (.+-.)-Ribasine. A Tandem Cyclization—Cycloaddition Route Leading to the Core Skeleton.

✍ Albert Padwa; Laura Precedo; Mark A. Semones 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB 👁 2 views

Model Studies Directed Toward the Total Synthesis of (±)-Ribasine. A Tandem Cyclization-Cycloaddition Route Leading to the Core Skeleton. -A tandem cyclization-cycloaddition sequence of model compound (II) represents a useful approach towards the synthesis of the oxabicyclo[3.2.1]octane ring system