✦ LIBER ✦

Synthesis of methyl (5Z,8Z,10E,12E,14Z)-eicosapentaenoate

✍ Scribed by Yasser M.A. Mohamed; Trond Vidar Hansen

Publisher: Elsevier Science
Year: 2011
Tongue: French
Weight: 263 KB
Volume: 52
Category: Article
ISSN: 0040-4039
DOI: 10.1016/j.tetlet.2010.12.078

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis of methyl (5Z, 8Z, 11Z, 14Z, 1

Synthesis of methyl (5Z, 8Z, 11Z, 14Z, 17E)-eicosapentaenoate and methyl (4Z, 7Z, 10Z, 13Z, 16Z, 19E)-docosahexaenoate

✍ Jean-Michel Vatèle; Huynh Dong Doan; Jean-Michel Chardigny; Jean-Louis Sébédio; 📂 Article 📅 1994 🏛 Elsevier Science 🌐 English ⚖ 708 KB

3Z,6Z,9Z,12E)-Pentadecatetraenal, a common intermediate in the synthesis of methyl A l7t EPA and methyl A I9t DHA, was obtained by copper(I)-catalyzed coupling between the Grignard reagent of I, 1-diethoxy-3-butyne and (Z, E)l-bromo-5,8-undecadien-2-yne followed by semi-hydrogenation of the resultin

Synthesis of methyl (5Z,8Z,11Z,14Z,17Z)-

Synthesis of methyl (5Z,8Z,11Z,14Z,17Z)- and (5Z,8Z,11Z,14Z,17E)-[18-14C] eicosapentaenoate

✍ Thierry Eynard; Didier Poullain; Jean-Michel Vatèle; Jean-Pierre Noël; Jean-Mich 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 French ⚖ 548 KB

Synthesis of methyl (5Z, 8Z, 11E, 14Z, 1

Synthesis of methyl (5Z, 8Z, 11E, 14Z, 17Z)- and (5Z, 8Z, 11E, 14Z, 17E)-eicosapentaenoate (EPA Δ 11t and Δ11t, 17t)

✍ Jean-Michel Vatèle; Huynh Dong Doan; Bernard Fenet; Jean-Michel Chardigny; Jean- 📂 Article 📅 1995 🏛 Elsevier Science 🌐 English ⚖ 407 KB

Chemistry and Physics of LIPIDS Synthesis of methyl (5Z,8Z,11E,14Z,17Z)and (5Z,8Z,11E,14Z,17E)-eicosapentaenoate (EPA Allt and A1 lt,17t)

Synthesis of (9Z,12E)- and (9E,12Z)-[1-1

Synthesis of (9Z,12E)- and (9E,12Z)-[1-14C]linoleic acid and (5Z,8Z,11Z,14E)-[1-14C]arachidonic ácid

✍ Olivier Berdeaux; Jean-Michel Vatèle; Thierry Eynard; Mohammed Nour; Didier Poul 📂 Article 📅 1995 🏛 Elsevier Science 🌐 English ⚖ 741 KB

3Z,6E)-l-Bromododeca-3,6-diene, a common intermediate in the synthesis of labelled 12t linoleic acid and 14t arachidonic acid, was obtained from (E)-3-nonyl-l-ol, in four steps, via conventional functional manipulations. Cross-coupling of this bromododecadiene with the Grignard reagent of l-chloro-5

Enantiospecific synthesis of isomeric8,9

Enantiospecific synthesis of isomeric8,9,12-trihydroxyeicosa-5(Z),10(E),14(Z)-trienoic acids

✍ Pendri Yadagiri; Dong-Soo Shin; J.R. Falck 📂 Article 📅 1988 🏛 Elsevier Science 🌐 French ⚖ 253 KB

Five stereoisomers of trio1 2, an arachidonic acid metabolite isolated from platelets, were prepared using a convergent strategy based on 8-oxido ylide homologation of a carbohydrate-derived precursor. Trioxilins 2 and 3 were isolated initially from mammalian platelets by Jones et al1 who proposed t

Synthesis of (2Z,6Z,10Z,14E,18E)-farnesy

Synthesis of (2Z,6Z,10Z,14E,18E)-farnesylfarnesol,

✍ Alexander M. Moiseenkov; Evgeni V. Polunin; Alexei V. Semenovsky 📂 Article 📅 1981 🏛 Elsevier Science 🌐 French ⚖ 498 KB

using a two-stage cis-C5-homologation procedure is described. During recent years, much attention has been given to polyprenols, mainly due to their importance as lipophilic, membrane-soluble carbohydrate carriers in the biosynthesis of both bacterial cell wall polysaccharides and prokaryotic and eu