𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A Concise and Stereoselective Synthesis of Squalamine

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

Book ID
125510732
Publisher
American Chemical Society
Year
2003
Tongue
English
Weight
56 KB
Volume
5
Category
Article
ISSN
1523-7060

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Stereoselective synthesis of squalamine
Stereoselective synthesis of squalamine dessulfate
✍ Robert M. Moriarty; Livia A. Enache; William A. Kinney; Craig S. Allen; James W. πŸ“‚ Article πŸ“… 1995 πŸ› Elsevier Science 🌐 French βš– 212 KB
A Short and Highly Stereoselective Synth
A Short and Highly Stereoselective Synthesis of Squalamine from Methyl Chenodeoxycholanate
✍ 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

A concise, stereoselective synthesis of
A concise, stereoselective synthesis of (Β±)-geissoschizine
✍ M.-LluΓ―sa Bennasar; Juan-Miguel JimΓ©nez; Bilal A. Sufi; Joan Bosch πŸ“‚ Article πŸ“… 1996 πŸ› Elsevier Science 🌐 French βš– 126 KB

A stereocontrolled synthesis of (-+)-geissoschizine, involving the addition of the enolate derived from l-acetylindole to pyridinium salt 2, cyclization of the resultant 1,4-dihydropyridine, stereoselective elaboration of the E-ethylidene substituent, closure of C ring by Pummerer reaction, and meth