✦ LIBER ✦

Syntheses and Evaluation of Simplified Pretubulysin Analogues

✍ Scribed by Jens L. Burkhart; Rolf Müller; Uli Kazmaier

Publisher: John Wiley and Sons
Year: 2011
Tongue: English
Weight: 503 KB
Volume: 2011
Category: Article
ISSN: 1434-193X
DOI: 10.1002/ejoc.201100155

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis and Biological Evaluation of P

Synthesis and Biological Evaluation of Pretubulysin and Derivatives

✍ Angelika Ullrich; Jennifer Herrmann; Rolf Müller; Uli Kazmaier 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 318 KB 👁 1 views

ChemInform Abstract: Syntheses and Biolo

ChemInform Abstract: Syntheses and Biological Evaluation of (+)-Lactacystin and Analogues

✍ Craig E. Masse; Adam J. Morgan; Julian Adams; James S. Panek 📂 Article 📅 2001 🏛 John Wiley and Sons ⚖ 24 KB 👁 1 views

Syntheses and Biological Evaluation of I

Syntheses and Biological Evaluation of Iriomoteolide 3a and Analogues

✍ Riccardo Cribiú; Corinna Jäger; Cristina Nevado 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 402 KB 👁 2 views

ChemInform Abstract: Syntheses and Biolo

ChemInform Abstract: Syntheses and Biological Evaluation of Two New Naproxen Analogues.

✍ K. W. JUNG; K. D. JANDA; P. J. SANFILIPPO; M. WACHTER 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB 👁 2 views

ChemInform Abstract: Syntheses and Biolo

ChemInform Abstract: Syntheses and Biological Evaluation of Ring-C Modified Colchicine Analogues.

✍ Baiyuan Yang; Zhiqing C. Zhu; Holly V. Goodson; Marvin J. Miller 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB 👁 2 views

Stereoselective Synthesis of Structurall

Stereoselective Synthesis of Structurally Simplified Cephalostatin Analogues by Multiple Heck Reactions and Their Biological Evaluation

✍ Lutz F. Tietze; Wolf-Rüdiger Krahnert 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 296 KB

The stereoselective synthesis of structurally simplified heptacyclic cephalostatin analogues 2, 3, 18-21, 31, 32 and 33 by multiple Heck reactions is described. The key step of the synthesis is a selective Heck reaction of hydrindene 7 with 12 and 25, respectively at the vinyl bromide moiety followe