𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Total Synthesis of Halipeptins A and D and Analogues

✍ Scribed by K. C. Nicolaou; David W. Kim; Daniel Schlawe; Dimitrios E. Lizos; Rita G. de Noronha; Deborah A. Longbottom

Publisher
John Wiley and Sons
Year
2005
Tongue
English
Weight
155 KB
Volume
117
Category
Article
ISSN
0044-8249

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Total Synthesis of Halipeptins A and D a
Total Synthesis of Halipeptins A and D and Analogues
✍ K. C. Nicolaou; David W. Kim; Daniel Schlawe; Dimitrios E. Lizos; Rita G. de Nor πŸ“‚ Article πŸ“… 2005 πŸ› John Wiley and Sons 🌐 English βš– 156 KB πŸ‘ 1 views
Total Synthesis of Pederin and Analogues
Total Synthesis of Pederin and Analogues
✍ Dr. Fanghui Wu; Dr. Michael E. Green; Prof.β€…Dr. Paul E. Floreancig πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons 🌐 English βš– 280 KB πŸ‘ 1 views
Total Synthesis of Pederin and Analogues
Total Synthesis of Pederin and Analogues
✍ Dr. Fanghui Wu; Dr. Michael E. Green; Prof.β€…Dr. Paul E. Floreancig πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons 🌐 English βš– 290 KB πŸ‘ 1 views
Total Synthesis of Halipeptin A: A Poten
Total Synthesis of Halipeptin A: A Potent Antiinflammatory Cyclic Depsipeptide
✍ Shouyun Yu; Xianhua Pan; Xianfeng Lin; Dawei Ma πŸ“‚ Article πŸ“… 2005 πŸ› John Wiley and Sons 🌐 English βš– 182 KB πŸ‘ 1 views

The halipeptins A (1) and B (2) are two cyclic depsipeptides that were isolated from the sponge Haliclona species by Gomez-Paloma and co-workers. [1,2] Initially, their structures were misassigned as the 17-membered cyclic depsipeptides containing an unusual oxazetidine. [1] One year later the same

Apoptolidin A: Total Synthesis and Parti
Apoptolidin A: Total Synthesis and Partially Glycosylated Analogues
✍ Hermut Wehlan; Mario Dauber; M. Teresa Mujica Fernaud; Julia Schuppan; Sonja Kei πŸ“‚ Article πŸ“… 2006 πŸ› John Wiley and Sons 🌐 English βš– 458 KB

## Abstract The total synthesis of apoptolidin A is described employing an early glycosylation strategy. Strategic disconnections were chosen between C11–C12 (cross‐coupling) and C19O–C1 (macrocyclization). The __cis__‐selective glycosylation at C9‐OH was achieved with the new SIBA protective group