✦ LIBER ✦

Distribution and decarboxylation of 114Ciodoacetic acid in dogs

✍ Scribed by K.R. Brody; R.P. Spencer

Publisher: Elsevier Science
Year: 1972
Weight: 451 KB
Volume: 23
Category: Article
ISSN: 0020-708X
DOI: 10.1016/0020-708x(72)90125-1

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Measurement and correlation of the solub

Measurement and correlation of the solubility of 1-alkanols (C14, C16), in n-alkanes (C7C16)

✍ Urszula Domańska 📂 Article 📅 1996 🏛 Elsevier Science 🌐 English ⚖ 741 KB

Stereochemical dependence of the vicinal

Stereochemical dependence of the vicinal 13C′NCα1H and 1HCαC′15N proton-heteroatom coupling constants in the NMR spectra of peptides. Comparison of experimental and theoretical data

✍ V.F Bystrov; Yu.D Gavrilov; V.N Solkan 📂 Article 📅 1975 🏛 Elsevier Science ⚖ 401 KB

Absorption, tissue distribution, and exc

Absorption, tissue distribution, and excretion of bunolol-14C by dogs

✍ Franz-Josef Leinweber; Lloyd J. Haynes; Malcolm C. Crew; Frederick J. Di Carlo 📂 Article 📅 1971 🏛 John Wiley and Sons 🌐 English ⚖ 444 KB

Absorption, distribution and excretion o

Absorption, distribution and excretion of 14C-meglumine in rats and dogs after administration of 14C-meglumine salicylate

✍ Joel F. Heeg; Gordon S. Born; Wayne V. Kessler; Stanley M. Shaw; Winthrop E. Lan 📂 Article 📅 1977 🏛 John Wiley and Sons 🌐 English ⚖ 526 KB

Meglumine labeled with carbon-14 was administered orally as 14C-meglumine salicylate to rats and dogs to study its distribution and excretion. The compound was incompletely absorbed; that which was absorbed was rapidly excreted in the urine. Peak blood levels were about 5-10 mug/ml in rats and 2-8 m

Transamidination of [1-14C]-guanidinoace

Transamidination of [1-14C]-guanidinoacetic acid to14C-glycine and decarboxylation to14CO2in white spruce shoot primordia entering winter dormancy

✍ Don J. Durzan 📂 Article 📅 2009 🏛 Springer-Verlag 🌐 English ⚖ 221 KB

Studies in marine macrolide synthesis: S

Studies in marine macrolide synthesis: Stereocontrolled synthesis of the C1C11 and C15C27 subunits of aplyronine A

✍ Ian Paterson; Cameron J Cowden; Michael D Woodrow 📂 Article 📅 1998 🏛 Elsevier Science 🌐 French ⚖ 231 KB

The aplyronine C I-CII subunit 4, containing 4 stereocentres and the (E,E)-diene system, was prepared in 7 steps from ethyl ketone (R)-8 using a boron-mediated anti aldol reaction. The corresponding C 15-C27 subunit 5, containing 6 stereogenic centres and an (E)-alkene, was obtained in 10 steps from