✦ LIBER ✦

Synthesis of tritium-labeled Ganciclovir

✍ Scribed by G. V. Sidorov; N. F. Myasoedov

Book ID: 111456175
Publisher: Springer
Year: 2011
Tongue: English
Weight: 135 KB
Volume: 53
Category: Article
ISSN: 1066-3622
DOI: 10.1134/s1066362211060130

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis of tritium-labeled phytohormon

Synthesis of tritium-labeled phytohormones

✍ Kh. K. Ablyanov; G. V. Sidorov; O. N. Beshkurova; A. A. Takanaev; Sh. I. Salikho 📂 Article 📅 1992 🏛 Springer 🌐 English ⚖ 337 KB

Synthesis of tritium-labeled Semax

✍ V. P. Shevchenko; I. Yu. Nagaev; L. Yu. Alfeeva; L. A. Andreeva; P. A. Klimova; 📂 Article 📅 2006 🏛 Springer 🌐 English ⚖ 124 KB

Synthesis of tritium-labeled Selank

✍ V. P. Shevchenko; I. Yu. Nagaev; L. Yu. Alfeeva; L. A. Andreeva; K. V. Shevchenk 📂 Article 📅 2006 🏛 Springer 🌐 English ⚖ 60 KB

Synthesis of tritium labeled mazindol

✍ Harry A. Dugger; Kenrick C. Tabot 📂 Article 📅 1976 🏛 John Wiley and Sons 🌐 French ⚖ 326 KB 👁 1 views

## Abstract Mazindol was labeled with tritium in the 6,9 positions in low yield starting with dimethyl phthalate‐3,6‐^3^H which was prepared by reduction of dimethyl 3‐chlorophthalate with tritium gas using 10% palladium on charcoal as a catalyst. The labeled dimethyl phathalate was hydrolisized wi

Synthesis of tritium-labeled bilirubin

✍ Bachir Latli; Matt Hrapchak; Dhileepkumar Krishnamurthy; Chris H. Senanayake 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 French ⚖ 153 KB

## Abstract Tritium‐labeled bilirubin with specific activities ranging from 6.8 to 8.8 Ci/mmol was prepared in a single step by reducing biliverdin dihydrochloride with sodium borotritide in ethanol. Copyright © 2008 John Wiley & Sons, Ltd.

Synthesis of tritium labeled zomepirac

✍ David C. Hoerr; Ann T. Scharf; John R. Carson; Larry E. Weaner 📂 Article 📅 1983 🏛 John Wiley and Sons 🌐 French ⚖ 378 KB 👁 1 views

## Abstract Tritium labeled zomepirac with a specific activity of 85 Ci/mol was prepared by selective alkylation of the penultimate desmethyl precursor using methyl iodide‐^3^H~3~. The alkylation reaction was explored using various bases and solvent media.