77376-03-5Relevant academic research and scientific papers
Substituted 2-nitrobenzyltrichloroacetate esters for photodirected oligonucleotide detritylation in solid films
Serafinowski, Pawel J.,Garland, Peter B.
supporting information; experimental part, p. 3284 - 3291 (2009/02/05)
Oligonucleotide microarray fabrication by chemical synthesis using photoacid generators in solid films could have advantages over existing methods, but has not matched the accuracy of conventional synthesis where detritylation is performed with acid solut
O-nitrobenzyl photolabile protecting groups with red-shifted absorption: Syntheses and uncaging cross-sections for one- And two-photon excitation
Aujard, Isabelle,Benbrahim, Chouaha,Gouget, Marine,Ruel, Odile,Baudin, Jean-Bernard,Neveu, Pierre,Jullien, Ludovic
, p. 6865 - 6879 (2007/10/03)
We evaluated the o-nitrobenzyl platform for designing photolabile protecting groups with red-shifted absorption that could be photolyzed upon one- and two-photon excitation. Several synthetic pathways to build different conjugated o-nitrobenzyl backbones,
PROPIONAMIDE DERIVATIVES USEFUL AS ANDROGEN RECEPTOR MODULATORS
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Page 40, (2010/02/10)
Compounds of formula (I) wherein R1 to R4, X and A are as defined in the claims and pharmaceutically acceptable salts and esters thereof, are disclosed. The compounds of formula (I) possess utility as tissue-selective androgen receptor modulators (SARM) and are useful in hormonal therapy, e.g. in the treatment or prevention of male hypogonadism and age-related conditions such as andropause.
γ-L-glutamyl-4-nitroanilide derivatives and process for determining γ-GTP activity using the same
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, (2008/06/13)
A γ-L-glutamyl-4-nitroanilide derivative of the formula: STR1 wherein R is a lower hydroxyalkyl group, is suitable as a substrate for determining γ-GTP activity.
