✦ LIBER ✦

A simple procedure for the synthesis of high specific activity tritiated (6S)-5-formyltetrahydrofolate

✍ Scribed by Richard G. Moran; Paul D. Colman

Publisher: Elsevier Science
Year: 1982
Tongue: English
Weight: 756 KB
Volume: 122
Category: Article
ISSN: 0003-2697
DOI: 10.1016/0003-2697(82)90252-4

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

The synthesis of tritiated methoxamine w

The synthesis of tritiated methoxamine with high specific activity

✍ R. M. Demarinis; A. J. Villani; D. Brungard; J. Meier 📂 Article 📅 1982 🏛 John Wiley and Sons 🌐 French ⚖ 153 KB

## Abstract Tritiated methoxamine with a specific activity of 28.5 Ci/mmol was prepared by iodination of methoxamine followed by catalytic tritiation.

Synthesis of high specific activity radi

Synthesis of high specific activity radiohalogenated amphetamine analogues for studies of the serotonin 5-HT2 receptor

✍ C.A. Mathis; J.M. Gerdes; A.T. Shulgin; A.J. Hoffman; D.E. Nichols 📂 Article 📅 1989 🏛 John Wiley and Sons 🌐 French ⚖ 143 KB

A method for the chemical synthesis of 1

A method for the chemical synthesis of 14C-labeled fatty acyl coenzyme A's of high specific activity

✍ James E. Bishop; Amiya K. Hajra 📂 Article 📅 1980 🏛 Elsevier Science 🌐 English ⚖ 537 KB

A simple and reliable method, based on that described by W. Seubert (1960, Biochem Prep. 7, 80-83), has been developed for the chemical synthesis of radioactive acyl coenzyme A's. I-14C-labeled fatty acids (palmitic, oleic, and linoleic) are converted to their acyl chlorides with oxalyl chloride. Th

Synthesis of deoxyadenosine-5′-(35S)-thi

Synthesis of deoxyadenosine-5′-(35S)-thiomonophosphate [dAMP(35S)] of high specific activity – a key intermediate for the synthesis of Sp-deoxyadenosine-5′-(alpha;-35S)-thiotriphosphate [Sp-dATP (α-35S)]

✍ K. M. Mathew; S. Ravi; C. V. Sontakke; H. Chander 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 French ⚖ 107 KB

## Abstract Unprotected deoxyadenosine **1** was treated with an excess of phosphorus acid and stoichiometric proportions of __N__, __N__′‐di‐__p__‐tolylcarbodiimide in anhydrous pyridine to give deoxyadenosine‐5′‐monophosphite **2**. The latter was activated with trimethylsilyl chloride followed b

The novel synthesis of the protease inhi

The novel synthesis of the protease inhibitor (S)-1-chloro-3-[(p-tolylsulfonyl)amino]-7-amino-2-[5,5,6,6-3H]heptanone ([3H]TLCK) labeled to high specific activity with tritium

✍ A. J. Villani; J. R. Heys 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 French ⚖ 466 KB 👁 2 views

Synthesis of high specific activity 80mB

Synthesis of high specific activity 80mBr and 123I labeled 5-halodeoxyuridines and other 80mBr compounds for the study of auger electron toxicity

✍ Rc Mease; Sj Gatley; Am Friedman 📂 Article 📅 1991 🏛 John Wiley and Sons 🌐 French ⚖ 458 KB

## Abstract Convenient preparations of ^80m^Br and ^123^I‐labeled 5‐halodeoxyuridines, required for basic investigations of Auger electron radiotoxicity, are described. These radioactive thymidine analogs were synthesized from deoxyuridine, radiohalide and N‐chlorosuccinimide in dilute sulfuric aci