Decorated Macrocycles via Ring-Closing Double-Reductive Amination. Identification of an Apoptosis Inducer of Leukemic Cells That at Least Partially Antagonizes a 5 …

…, A Negi, A Samali, E Szegezdi, PV Murphy

Index: Matos, Marie-Christine; Murphy, Paul V. Journal of Organic Chemistry, 2007 , vol. 72, # 5 p. 1803 - 1806

Full Text: HTML

Citation Number: 1

Abstract

A build–couple–pair strategy, including double-reductive amination macrocyclization, has been used to generate decorated macrocycles (eannaphanes) with an embedded triazole and monosaccharide. Biological screening led to the identification of an inducer of apoptosis

Related Articles:

Pd/P (t-Bu) 3: a mild and general catalyst for Stille reactions of aryl chlorides and aryl bromides

[Littke, Adam F.; Schwarz, Lothar; Fu, Gregory C. Journal of the American Chemical Society, 2002 , vol. 124, # 22 p. 6343 - 6348]

An easy access to styrenes: trans aryl 1, 3-, 1, 4-and 1, 5-dienes, and 1, 3, 5-trienes by Hiyama cross-coupling catalyzed by palladium nanoparticles

[Chatterjee, Tanmay; Dey, Raju; Ranu, Brindaban C. New Journal of Chemistry, 2011 , vol. 35, # 5 p. 1103 - 1110]

More Articles...