✦ LIBER ✦

The total synthesis and metabolism of 7,10,13,16-docosatetraenoate in the rat

✍ Scribed by Howard Sprecher

Book ID: 115735639
Publisher: Elsevier Science
Year: 1967
Tongue: English
Weight: 713 KB
Volume: 144
Category: Article
ISSN: 0005-2760
DOI: 10.1016/0005-2760(67)90159-2

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Reevaluation of the Pathway for the Meta

Reevaluation of the Pathway for the Metabolism of 7,10,13,16-Docosatetraenoic Acid to 4,7,10,13,16-Docosapentaenoic Acid in Rat-Liver

✍ B.S. Mohammed; S. Sankarappa; M. Geiger; H. Sprecher 📂 Article 📅 1995 🏛 Elsevier Science 🌐 English ⚖ 544 KB

The total synthesis and metabolism of oc

The total synthesis and metabolism of octadeca-5,8,11-trienoate, eicosa-10,13-dienoate and eicosa-7,10,13-trienoate in the fat-deficient rat

✍ Howard W. Sprecher 📂 Article 📅 1971 🏛 Elsevier Science 🌐 English ⚖ 769 KB

The metabolism of 4,7,10,13,16-[5-14c]do

The metabolism of 4,7,10,13,16-[5-14c]docosapentaenoic acid in the testis of the rat

✍ Raymond B. Bridges; John G. Coniglio 📂 Article 📅 1970 🏛 Elsevier Science 🌐 English ⚖ 500 KB

The synthesis of chiral derivatives of 1

The synthesis of chiral derivatives of 1,4,7,10,13,16-hexaoxacyclooctadecane

✍ Çakil Erk 📂 Article 📅 1980 🏛 Springer 🌐 English ⚖ 147 KB

The crystal structures of 10-oxa-1,4,7-t

The crystal structures of 10-oxa-1,4,7-trithiacyclododecane, 7,10,13-trioxa-1,4-dithiacyclopentadecane, 7,10,13,16-tetraoxa-1,4-dithiacyclooctadecane and 4,7,13,16-tetraoxa-1,10-dithiacyclooctadecane

✍ N. Kent Dalley; Steven B. Larson; Judith S. Smith; K. Lee Matheson; Reed M. Izat 📂 Article 📅 1981 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 339 KB

Synthesis of the macrocyclic thiocrown e

Synthesis of the macrocyclic thiocrown ethers 1,4,7,10,13,16,19-heptathiaheneicosane (21-S-7) and 1,4,7,10,13,16,19,22-octathiatetraeicosane (24-S-8)

✍ Jilles J.H. Edema; Jan Buter; Richard M. Kellogg 📂 Article 📅 1994 🏛 Elsevier Science 🌐 French ⚖ 248 KB

The synthesis and characterization of the two macrocyclic s&ides, 1,4,7,lO,l3,16,19-heptathiaheneicosane (21-S-7) and 1,4,7,10,13,16,19,22-octathiatetraeicosane (24-S-8), are describedstarting from different combmationsof dithiols and dichlorides of differing chain lengths. C&O, is used for the cycl