✦ LIBER ✦

A biogenetic-type synthesis of (±)-aplysiadiol, a brominated diterpene isolated from the marine mollusc aplysia kurodai

✍ Scribed by Haruki Niwa; Shigeru Ieda; Hideaki Inagaki; Kiyoyuki Yamada

Publisher: Elsevier Science
Year: 1990
Tongue: French
Weight: 151 KB
Volume: 31
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(00)97266-6

No coin nor oath required. For personal study only.

✦ Synopsis

f)-Aplysiadiol (1). a brominated diterpene having a ram, prenylated eudesmane skeleton was synthesized starting with (*)-hedycaryol(2) in a biogenetic manner.

Aplysiadiol(1) isolated ftom the Japanese marine mollusc ApZysti kurodai is a brominated diterpene having a rate, prenylated eudesmane skeleton.1) A biogenesis of aplysiadiol( 1) is shown in Scheme I. A prenylated germacrene-like precursor (A) biO8yMhe8ized from geranylgeranyl pyrophosphate (GGPP) may be

📜 SIMILAR VOLUMES

Isolation and structures of aplykurodins

Isolation and structures of aplykurodins a and b, two new isoprenoids from the marine mollusk aplysia kurodai

✍ T. Miyamoto; R. Higuchi; T. Komori; T. Fujioka; K. Mihashi 📂 Article 📅 1986 🏛 Elsevier Science 🌐 French ⚖ 213 KB

ChemInform Abstract: Synthesis of Aplyol

ChemInform Abstract: Synthesis of Aplyolide A, Ichthyotoxic Macrolide Isolated from the Skin of the Marine Mollusk Aplysia depilans.

✍ Aldo Spinella; Tonino Caruso; Marco Martino; Carmine Sessa 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 22 KB 👁 2 views