𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Total Synthesis of Marine Eicosanoid (−)-Hybridalactone

✍ Scribed by Koichiro Ota; Naoto Sugata; Yoshihiko Ohshiro; Dr. Etsuko Kawashima; Dr. Hiroaki Miyaoka

Book ID
115551523
Publisher
John Wiley and Sons
Year
2012
Tongue
English
Weight
479 KB
Volume
18
Category
Article
ISSN
0947-6539

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

The stereochemistry and biosynthesis of
The stereochemistry and biosynthesis of hybridalactone, an eicosanoid from laurencia hybrida
✍ E.J. Corey; Biswanath De; Jay W. Ponder; Jeremy M. Berg 📂 Article 📅 1984 🏛 Elsevier Science 🌐 French ⚖ 276 KB

The stereochemistry of the marine eicosanoid, hybrldalactone, has been determined experimentally to be as in 2, in accord with a proposed scheme of biosynthesis from eicosapentaenoic acid. Recently a novel eicosanoid, designated hybridalactone, was isolated from the marine alga Laurencia hybrida an

Synthesis of cyclopentane-containing mar
Synthesis of cyclopentane-containing marine eicosanoid bacillariolide II
✍ Hiroaki Miyaoka; Masahide Tamura; Yasuji Yamada 📂 Article 📅 1998 🏛 Elsevier Science 🌐 French ⚖ 223 KB

Marine eieosanoid bacillariolide II was synthesized from (R)-malic acid, involving the diastereoselective one-pot formation of chiral cyclopentane derivative 12 from the anion of allyl phenyl snlfone and chiral epoxymesylate 11 as the key step.