Synthesis of lipophilic paramagnetic contrast agents

…, DC Hill, JL Thompson, PA Petillo

Index: Baker, William C.; Choi, Michael J.; Hill, Daniel C.; Thompson, Julie L.; Petillo, Peter A. Journal of Organic Chemistry, 1999 , vol. 64, # 8 p. 2683 - 2689

Full Text: HTML

Citation Number: 44

Abstract

The facile, high-yielding synthesis of a series of macrocycles 7a-k in 75-100% yield is reported. The transformation of these compounds to their carboxymethylated analogues 8a- k in 75-90% yield and subsequent gadolinium complexes 9a-k provides a series of homologous neutral paramagnetic contrast agents (PCAs) with tunable lipophilicity. Alkylated cationic intermediates 6a-k are prepared in yields of 72-94% from glyoxal ...

Related Articles:

Expeditious N-monoalkylation of 1, 4, 7, 10-tetraazacyclododecane (cyclen) via formamido protection

[Boldrini; Giovenzana; Pagliarin; Palmisano; Sisti Tetrahedron Letters, 2000 , vol. 41, # 33 p. 6527 - 6530]

More Articles...