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Indole arylation studies directed towards the synthesis of simplified eastern subunits of chloropeptin and kistamycin

✍ Scribed by Annie-Claude Carbonnelle; Eduardo González Zamora; René Beugelmans; Georges Roussi

Book ID
104259372
Publisher
Elsevier Science
Year
1998
Tongue
French
Weight
238 KB
Volume
39
Category
Article
ISSN
0040-4039

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✦ Synopsis

Aryl indoles which are building blocks for the synthesis of simplified analogues of macropolypeptides containing an endo carbon-carbon bond are obtained by Suzuki Pal-catalyzed cross coupling reactions involving either haloindoles or indole boronic acids and properly meta substituted phenyl components.

📜 SIMILAR VOLUMES

The first synthesis of simplified 16- an
The first synthesis of simplified 16- and 17-membered ring macropolypeptides containing the phenyl-indole system of kistamycin and chloropeptin I, II
✍ Annie-Claude Carbonnelle; Eduardo González Zamora; René Beugelmans; Georges Rous 📂 Article 📅 1998 🏛 Elsevier Science 🌐 French ⚖ 125 KB

The .rynthesis of simplified 16-and 17-membered rin~ macropolvpeptides was achieved hv Ni ~ mediated carbon-carbon ring closure of properly substituted linear precursors.