✦ LIBER ✦

The total synthesis of d1-epiibogamine

✍ Scribed by Yoshio Ban; Takeshi Wakamatsu; Yasuo Fujimoto; Takeshi Oishi

Publisher: Elsevier Science
Year: 1968
Tongue: French
Weight: 207 KB
Volume: 9
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(00)89499-x

No coin nor oath required. For personal study only.

✦ Synopsis

The iboga alkaloids are not only unique in chemical structures (l), but also interesting in physiological activities (2). The total syntheses of dl-ibogamine(Ia) and dl-ibogaine(Ic), the representative members of these alkaloids, and of the corresponding C-4 epimers were al-

📜 SIMILAR VOLUMES

The total synthesis of d1-dihydrocallitr

The total synthesis of d1-dihydrocallitrisin

✍ Jollie D. Godfrey; Arthur G. Schultz 📂 Article 📅 1979 🏛 Elsevier Science 🌐 French ⚖ 205 KB

Bromodiene 2 is converted to dl-dihydrocallitrisin (l), a sesquiterpene lactone recently isolated from the heartwood oFCa11itris columellari?. We wish to describe the total synthesis of $I\_-dihydrocallitrisin (1\_), a new sesquiterpene lactone isolated by Carman and Brecknell from the heartwood of

A total synthesis of d1-cerulenin and d1

A total synthesis of d1-cerulenin and d1-tetrahydrocerulenin

✍ Ann A. Jakubowski; Frank S. Guziec Jr.; Max Tishler 📂 Article 📅 1977 🏛 Elsevier Science 🌐 French ⚖ 231 KB

Total synthesis of d1-hirsutic acid

✍ Hisanobu Hashimoto; Kazuo Tsuzuki; Fujio Sakan; Haruhisa Shirahama; Takeshi Mats 📂 Article 📅 1974 🏛 Elsevier Science 🌐 French ⚖ 170 KB

Although the skeleton of hirsutic acid [L)l,', a highly oxygenated fungal sesquiterpenoid, has already been synthesized 3,4 , the total synthesis of the acid has remained unsettled, because of the difficulty of constructing the densely functionalized system. Herein we describe a stereospecific conv

A total synthesis of d1-eburnamonine

✍ M.F. Bartlett; W.I. Taylor 📂 Article 📅 1959 🏛 Elsevier Science 🌐 French ⚖ 122 KB

Total synthesis of the antiinflammatory

Total synthesis of the antiinflammatory and proresolving protectin D1

✍ Narihito Ogawa; Yuichi Kobayashi 📂 Article 📅 2011 🏛 Elsevier Science 🌐 French ⚖ 580 KB

Stereoselective total synthesis of protectin D1 was completed through construction of the Z,E,E-triene structure by using the Suzuki coupling between the vinyl borane (C13-C22) and the vinyl iodide (C1-C12). The Z-enyne, the acetylene precursor of the vinyl borane was synthesized from optically acti

1,6-dihydro-3(2H)-pyridinones as synthet

1,6-dihydro-3(2H)-pyridinones as synthetic intermediates. A novel total synthesis of (±)-ibogamine and (±)-epiibogamine

✍ Takeshi Imanishi; Noriyuki Yagi; Hiroaki Shin; Miyoji Hanaoka 📂 Article 📅 1981 🏛 Elsevier Science 🌐 French ⚖ 234 KB