✦ LIBER ✦

Ingenamine alkaloids isolated from the sponge Xestospongia ingens: Structures and absolute configurations

✍ Scribed by Fangming Kong; Raymond J. Andersen

Publisher: Elsevier Science
Year: 1995
Tongue: French
Weight: 676 KB
Volume: 51
Category: Article
ISSN: 0040-4020
DOI: 10.1016/0040-4020(95)00043-8

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Ingenamine, a novel pentacyclic alkaloid

Ingenamine, a novel pentacyclic alkaloid from the marine sponge Xestospongia ingens

✍ Fangming Kong; Raymond J. Andersen; Theresa M. Allen 📂 Article 📅 1994 🏛 Elsevier Science 🌐 French ⚖ 479 KB

ChemInform Abstract: Motuporamines A—C,

ChemInform Abstract: Motuporamines A—C, Cytotoxic Alkaloids Isolated from the Marine Sponge Xestospongia exigua (Kirkpatrick).

✍ D. E. WILLIAMS; P. LASSOTA; R. J. ANDERSEN 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 27 KB 👁 2 views

ChemInform Abstract: Motuporamines, Anti

ChemInform Abstract: Motuporamines, Antiinvasion and Antiangiogenic Alkaloids from the Marine Sponge Xestospongia exigua (Kirkpatrick): Isolation, Structure Elucidation, Analogue Synthesis, and Conformational Analysis.

✍ David E. Williams; Kyle S. Craig; Brian Patrick; Lianne M. McHardy; Rob van Soes 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB 👁 2 views

ChemInform Abstract: Synthesis and Absol

ChemInform Abstract: Synthesis and Absolute Configuration of Stellettadine A, a Bisguanidinium Alkaloid Isolated from a Marine Sponge Stelletta sp.

✍ Hirosato Takikawa; Dai Nozawa; Kenji Mori 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB 👁 2 views

Aragusterols E-H, new 26,27-cyclosterols

Aragusterols E-H, new 26,27-cyclosterols from the Okinawan marine sponge of the genus Xestospongia and absolute configurations of xestokerols A and B

✍ Hiroaki Miyaoka; Masakazu Shinohara; Masako Shimomura; Hidemichi Mitome; Akiko Y 📂 Article 📅 1997 🏛 Elsevier Science 🌐 French ⚖ 612 KB

New 26, 27-cyclosterols, aragusterols E-H, were isolated from the Okinawan marine sponge of the genus Xestospongia. Their structures were determined by spectroscopic measurement and chemical conversion. The absolute configurations of xestokerols A and B were determined by chemical conversion.

ChemInform Abstract: Aragusterols E-H, N

ChemInform Abstract: Aragusterols E-H, New 26,27-Cyclosterols from the Okinawan Marine Sponge of the Genus Xestospongia and Absolute Configurations of Xestokerols A and B.

✍ H. MIYAOKA; M. SHINOHARA; M. SHIMOMURA; H. MITOME; A. YANO; K. IGUCHI; Y. YAMADA 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB 👁 1 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v