99277-71-1Relevant articles and documents
Synthesis and solid-phase purification of anthranilic sulfonamides as CCK-2 ligands
Woods, Craig R.,Hack, Michael D.,Allison, Brett D.,Phuong, Victor K.,Rosen, Mark D.,Morton, Magda F.,Prendergast, Clodagh E.,Barrett, Terrance D.,Shankley, Nigel P.,Rabinowitz, Michael H.
, p. 6905 - 6909 (2008/04/07)
A novel strategy for the synthesis of cholecystokinin-2 receptor ligands was developed. The route employs a solution-phase synthesis of a series of anthranilic sulfonamides followed by a resin capture purification strategy to produce multi-milligram quant
GLYCOGEN PHOSPHORYLASE INHIBITOR COMPOUNDS AND PHARMACEUTICAL COMPOSITIONS THEREOF
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Page/Page column 87-88, (2010/11/30)
The invention relates to glycogen phosphorylase inhibitor compounds, pharmaceutical compositions of these compounds, methods of treatment using the pharmaceutical compositions to treat diabetes, conditions associated with diabetes, and/or tissue ischemia,
Oxidation of 4-halo-2-nitrotoluene with tetrabutylammonium permanganate in pyridine: Development and safety evaluation
Deng, Xiaohu,Stefanick, Stephen,Pippel, Marna C. W.,Mani, Neelakandha S.
, p. 1287 - 1291 (2012/12/23)
4-Halo-2-nitrobenzoic acids are synthesized by oxidation of 4-halo-2-nitrotoluene with tetrabutylammonium permanganate (TBAP) in pyridine in multigram quantities. A significant induction period is observed at room temperature, and the vigorous exothermic