✦ LIBER ✦

Formal Synthesis of Squalamine from Desmosterol.

✍ Scribed by Kazuo Okumura; Yutaka Nakamura; Seiji Takeuchi; Isao Kato; Yoshinori Fujimoto; Nobuo Ikekawa

Book ID: 101951092
Publisher: John Wiley and Sons
Year: 2004
Weight: 142 KB
Volume: 35
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.200411170

No coin nor oath required. For personal study only.

✦ Synopsis

Abstract

For Abstract see ChemInform Abstract in Full Text.

📜 SIMILAR VOLUMES

A Short Formal Synthesis of Squalamine f

A Short Formal Synthesis of Squalamine from a Microbial Metabolite

✍ Kinney, William A.; Zhang, Xuehai; Williams, Jon I.; Johnston, Sean; Michalak, R 📂 Article 📅 2000 🏛 American Chemical Society 🌐 English ⚖ 31 KB

ChemInform Abstract: A Short Formal Synt

ChemInform Abstract: A Short Formal Synthesis of Squalamine from a Microbial Metabolite.

✍ William A. Kinney; Xuehai Zhang; Jon I. Williams; Sean Johnston; Ronald S. Micha 📂 Article 📅 2001 🏛 John Wiley and Sons ⚖ 31 KB 👁 2 views

Synthesis of desmosterol and epidesmoste

Synthesis of desmosterol and epidesmosterol from hyodeoxycholic acid

✍ Kiyoshige Ochi; Isao Matsunaga; Minoru Shindo; Chikara Kaneko 📂 Article 📅 1977 🏛 Elsevier Science 🌐 English ⚖ 474 KB

Stereoselective synthesis of squalamine

Stereoselective synthesis of squalamine dessulfate

✍ Robert M. Moriarty; Livia A. Enache; William A. Kinney; Craig S. Allen; James W. 📂 Article 📅 1995 🏛 Elsevier Science 🌐 French ⚖ 212 KB

Synthesis of squalamine. A steroidal ant

Synthesis of squalamine. A steroidal antibiotic from the shark

✍ Robert M. Moriarty; Sudersan M. Tuladhar; Liang Guo; Suzanne Wehrli 📂 Article 📅 1994 🏛 Elsevier Science 🌐 French ⚖ 275 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 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 76 KB 👁 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 7α,24R-dihydroxy-cholestan-3-one (9) was synthesized by using improved dehydrogenation of 4 followed by conjugate reduction and e