𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A Concise and Stereoselective Synthesis of Squalamine.

✍ Scribed by Dong-Hui Zhang; Feng Cai; Xiang-Dong Zhou; Wei-Shan Zhou


Publisher
John Wiley and Sons
Year
2003
Weight
78 KB
Volume
34
Category
Article
ISSN
0931-7597

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


A Short and Highly Stereoselective Synth
✍ Zhang Dong-Hui; Cai Feng; Zhou Xiang-Dong; Zhou Wei-Shan πŸ“‚ Article πŸ“… 2005 πŸ› John Wiley and Sons 🌐 English βš– 76 KB πŸ‘ 2 views

A short and highly stereoselective synthesis of squalamine (1) was accomplished in 9 steps from easily available methyl chenodeoxycholanate (2). The advanced intermediate 7Ξ±,24R-dihydroxy-cholestan-3-one (9) was synthesized by using improved dehydrogenation of 4 followed by conjugate reduction and e

ChemInform Abstract: A Concise, Stereose
✍ M.-L. BENNASAR; J.-M. JIMENEZ; B. A. SUFI; J. BOSCH πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 32 KB πŸ‘ 2 views

A Concise, Stereoselective Synthesis of (Β±)-Geissoschizine. -The stereoselective synthesis of (Β±)-geissoschizine (VIII) is based on the addition of the enolate derived from 1-acetylindole (I) to the pyridinium salt (II) and cyclization of the resultant 1,4-dihydropyridine. -(BENNASAR, M.-L.;

A Concise Stereoselective Synthesis of 2
✍ Tarun K. Pradhan; Antoine Joosten; Jean-Luc Vasse; Philippe Bertus; Philippe Kar πŸ“‚ Article πŸ“… 2009 πŸ› John Wiley and Sons 🌐 English βš– 199 KB

## Abstract A simple and stereoselective method for the preparation of (__Z__)‐2‐substituted 1‐aminocyclopropanecarboxylic acids is described. The common key step for these reaction sequences involves the stereoselective Ti‐mediated coupling of benzyloxy nitrile and homoallylic alcohol. The resulti