✦ LIBER ✦

The absolute configuration of avarol, a rearranged sesquiterpenoid hydroquinone from a marine sponge

✍ Scribed by de Rosa, Salvatore; Minale, Luigi; Riccio, Raffaele; Sodano, Guido

Book ID: 121000318
Publisher: Royal Society of Chemistry
Year: 1976
Weight: 948 KB
Volume: 13
Category: Article
ISSN: 1472-7781
DOI: 10.1039/P19760001408

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Avarol a novel sesquiterpenoid hydroquin

Avarol a novel sesquiterpenoid hydroquinone with a rearranged drimane skeleton from the sponge disidea avara

✍ L. Minale; R. Riccio; G. Sodano 📂 Article 📅 1974 🏛 Elsevier Science 🌐 French ⚖ 246 KB

Laboratorio per la Chimica delle molecole di interesse biologic0 de1 C.N.N.

Antimicrobial activity of avarol, a sesq

Antimicrobial activity of avarol, a sesquiterpenoid hydroquinone from the marine sponge, dysidea avara

✍ Cariello, Lucio; Zanetti, Laura; Cuomo, Vincenzo; Vanzanella, Fortunato 📂 Article 📅 1982 🏛 Elsevier Science 🌐 English ⚖ 177 KB

Total Synthesis of (+)-Strongylin A, a R

Total Synthesis of (+)-Strongylin A, a Rearranged Sesquiterpenoid Hydroquinone from a Marine Sponge

✍ Kamishima, Takaaki; Kikuchi, Takuya; Katoh, Tadashi 📂 Article 📅 2013 🏛 John Wiley and Sons 🌐 English ⚖ 489 KB

Avarol, a sesquiterpenoid hydroquinone f

Avarol, a sesquiterpenoid hydroquinone from Dysidea avara

✍ Puliti, R. ;De Rosa, S. ;Mattia, C. A. 📂 Article 📅 1994 🏛 International Union of Crystallography 🌐 English ⚖ 364 KB

Structure of the 2,5-dimethyl ether of a

Structure of the 2,5-dimethyl ether of avarol, a sesquiterpenoid hydroquinone from the marine sponge Dysidea avara

✍ Giordano, F. ;Puliti, R. 📂 Article 📅 1987 🏛 International Union of Crystallography 🌐 English ⚖ 426 KB

Structure and absolute configuration of

Structure and absolute configuration of a new rearranged chamigrane-type sesquiterpenoid from the sea hare Aplysia sp.

✍ Sergei N Fedorov; Larisa K Shubina; Anatoly I Kalinovsky; Ekaterina G Lyakhova; 📂 Article 📅 2000 🏛 Elsevier Science 🌐 French ⚖ 145 KB

6S,10S)-3,10- Dimethyl-7,11-dimethylidenespiro[5,5]undec-2-en-4-one (1), a new rearranged chamigrane-type sesquiterpenoid with two sp 2 -hybridized carbons in α-positions to the spiro-atom, was isolated from the alcoholic extract of the sea hare Aplysia sp. and its structure and absolute configurati