First unequivocal synthesis of dissymmetrical trans N,N′-difunctionalized 1,4,8,11-tetraazacyclotetradecane
✍ Scribed by Christophe Bucher; Guy Royal; Jean-Michel Barbe; Roger Guilard
- Book ID
- 104260986
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- French
- Weight
- 190 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
The first unequivocal synthesis of disymmetrical trans N,N'-difunctionalized tetraazamacrocycles in cyclam series is reported. This convenient four-step method can be used for the synthesis of various trans N,N'-difunctionalized tetraazamacrocycles bearing two different pendant donor arms.
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Synthesis of the Bifunctional Chelating Agent 6-(4-Aminobenzyl) -1,4,8,11-tetraazacyclotetradecane-N,N',N",N"'-tetraacetic Acid (H 2 NBn-TETA). -An improved procedure for the synthesis of the azamacrocyclic ligand (VII), used as a radionuclide carrier in cancer chemotherapy, is reported. Additionall