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The α,5-dicarboxy-2-nitrobenzyl caging group, a tool for biophysical applications with improved hydrophilicity: synthesis, photochemical properties and biological characterization.
Schaper K, Madani Mobarekeh SA, Doro P, Maydt D. Schaper K, et al. Photochem Photobiol. 2010 Nov-Dec;86(6):1247-54. doi: 10.1111/j.1751-1097.2010.00803.x. Epub 2010 Sep 29. Photochem Photobiol. 2010. PMID: 20880228
Earlier we reported on the synthesis of alpha,4-dicarboxy-2-nitrobenyzl caged compounds (Schaper, K. et al. [2002] Eur. J. Org. Chem., 1037-1046). These compounds have the advantage of an increased hydrophilicity compared with the well-established alpha-carboxy-2-ni …
Earlier we reported on the synthesis of alpha,4-dicarboxy-2-nitrobenyzl caged compounds (Schaper, K. et al. [2002] Eur. J. Org …
Structural assignment of adenine aggregates in CDCl3.
Biemann L, Häber T, Maydt D, Schaper K, Kleinermanns K. Biemann L, et al. Among authors: schaper k. J Chem Phys. 2008 May 21;128(19):195103. doi: 10.1063/1.2912064. J Chem Phys. 2008. PMID: 18500901
Theoretical investigation of the excited states of 2-nitrobenzyl and 4,5-methylendioxy-2-nitrobenzyl caging groups.
Schaper K, Etinski M, Fleig T. Schaper K, et al. Photochem Photobiol. 2009 Sep-Oct;85(5):1075-81. doi: 10.1111/j.1751-1097.2009.00560.x. Epub 2009 Apr 6. Photochem Photobiol. 2009. PMID: 19508640
However, even recently new side reactions have been discovered. Earlier, we reported [Bley, F., K. Schaper, and H. Gorner (2008), Photochem. Photobiol.84 162-171] that we found long-lived triplet states which do not lead to product formation for the bathochromic abs …
However, even recently new side reactions have been discovered. Earlier, we reported [Bley, F., K. Schaper, and H. Gorner (200 …
132 results