✦ LIBER ✦

Stereoselective synthesis of zoanthenol ABC-ring by radical strategy

✍ Scribed by Yamashita, Shuji; Suda, Naoki; Hayashi, Yujiro; Hirama, Masahiro

Book ID: 125452707
Publisher: Elsevier Science
Year: 2013
Tongue: French
Weight: 450 KB
Volume: 54
Category: Article
ISSN: 0040-4039
DOI: 10.1016/j.tetlet.2012.12.104

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Enantioselective Synthesis of the Fully

Enantioselective Synthesis of the Fully Functionalized ABC Ring of Zoanthenol

✍ Naoki Sugano; Yuuki Koizumi; Go Hirai; Hiroki Oguri; Shoji Kobayashi; Shuji Yama 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 379 KB

Convergent synthesis of the ABC-ring moi

Convergent synthesis of the ABC-ring moiety of zoanthenol: intramolecular Mizoroki–Heck reaction

✍ Go Hirai; Hiroki Oguri; Sameh M Moharram; Koji Koyama; Masahiro Hirama 📂 Article 📅 2001 🏛 Elsevier Science 🌐 French ⚖ 85 KB

The highly congested ABC-ring moiety of zoanthenol was stereoselectively synthesized via an alkoxylithium-mediated coupling between the A-ring and C-ring moieties followed by a Mizoroki-Heck-type ring closure.

Stereoselective Synthesis of the ABC Rin

Stereoselective Synthesis of the ABC Ring System of Norzoanthamine

✍ Ghosh, Subhash; Rivas, Fatima; Fischer, Derek; González, Miguel A.; Theodorakis, 📂 Article 📅 2004 🏛 American Chemical Society 🌐 English ⚖ 116 KB

ChemInform Abstract: Stereoselective Syn

ChemInform Abstract: Stereoselective Synthesis of ABC-Ring System of Hemibrevetoxin B.

✍ H. MATSUKURA; M. MORIMOTO; T. NAKATA 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 34 KB

Synthetic studies on brevetoxin-B. Part

Synthetic studies on brevetoxin-B. Part 1: Stereoselective synthesis of the ABC-ring system

✍ Goh Matsuo; Hiroko Matsukura; Nobuyuki Hori; Tadashi Nakata 📂 Article 📅 2000 🏛 Elsevier Science 🌐 French ⚖ 107 KB

Stereoselective synthesis of the tricycl

Stereoselective synthesis of the tricyclic core ABC-rings of nakadomarin and manzamine from a common intermediate

✍ Philip Magnus; Mark R Fielding; Charles Wells; Vince Lynch 📂 Article 📅 2002 🏛 Elsevier Science 🌐 French ⚖ 263 KB

Pauson-Khand cyclization of the enamide 9 proceeds in trifluoroethanol to give cyclopentenone 10, which on hydrogenation gives 11, having the core ABC-rings of nakadomarin 1.