✦ LIBER ✦

Synthesis of Substituted Phenols by Using the Ring-Closing Metathesis/Isoaromatization Approach

✍ Scribed by Kazuhiro Yoshida; Rintaro Narui; Tsuneo Imamoto

Publisher: John Wiley and Sons
Year: 2008
Tongue: English
Weight: 319 KB
Volume: 14
Category: Article
ISSN: 0947-6539
DOI: 10.1002/chem.200800943

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis of Medium-Sized Rings by the R

Synthesis of Medium-Sized Rings by the Ring-Closing Metathesis Reaction

✍ Martin E. Maier 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 150 KB 👁 2 views

General Approach for Template-Directed S

General Approach for Template-Directed Synthesis of Macroheterocycles by Ring-Closing Metathesis (RCM)

✍ Alexey V. Chuchuryukin; Preston A. Chase; Harm P. Dijkstra; Bart M. J. M. Suijke 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 228 KB 👁 1 views

A Double Ring-Closing Metathesis Approac

A Double Ring-Closing Metathesis Approach for the Synthesis of β-C-Trisaccharides

✍ Maarten H. D. Postema; Jared L. Piper; Venu Komanduri; Lei Liu 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 187 KB 👁 1 views

A Double Ring-Closing Metathesis Approac

A Double Ring-Closing Metathesis Approach for the Synthesis of β-C-Trisaccharides

✍ Maarten H. D. Postema; Jared L. Piper; Venu Komanduri; Lei Liu 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 186 KB 👁 1 views

Synthesis Mediated by Ring-Closing Metat

Synthesis Mediated by Ring-Closing Metathesis – Applications in the Synthesis of Azasugars and Alkaloids

✍ Upendra K. Pandit; Herman S. Overkleeft; Bennett C. Borer; Hans Bieräugel 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 440 KB 👁 2 views

The application of the ring-closing metathesis (RCM) castanospermine ( ) is presented. The utilisation of two RCM steps in the synthetic sequence leading to the multicyclic reaction to the construction of a wide variety of nitrogencontaining ring systems is described. The examples include ABCDE nucl

Stereoselective Synthesis of the Natural

Stereoselective Synthesis of the Naturally Occurring Lactones (−)-Osmundalactone and (−)-Muricatacine Using Ring-Closing Metathesis

✍ Miguel Carda; Santiago Rodríguez; Florenci González; Encarnación Castillo; Alici 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 150 KB 👁 1 views

The stereoselective synthesis of the naturally occurring lactones osmundalactone (-)-1 and muricatacin (-)-2 is described. The key steps in each synthesis are the stereoselective addition of a Grignard reagent to a suitably protected αhydroxy aldehyde and a ring-closing metathesis.