42036-59-9Relevant academic research and scientific papers
GLYCOLATE OXIDASE INHIBITORS FOR THE TREATMENT OF DISEASE
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, (2021/01/22)
Described herein are compounds, methods of making such compounds, pharmaceutical compositions and medicaments containing such compounds, and methods of using such compounds to treat or prevent diseases or disorders associated with a defect in glyoxylate metabolism, for example a disease or disorder associated with the enzyme glycolate oxidase (GO) or alterations in oxalate metabolism. Such diseases or disorders include, for example, disorders of glyoxylate metabolism, including primary hyperoxaluria, that are associated with production of excessive amounts of oxalate.
GLYCOLATE OXIDASE INHIBITORS FOR THE TREATMENT OF DISEASE
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, (2019/07/17)
Described herein are compounds, methods of making such compounds, pharmaceutical compositions and medicaments containing such compounds, and methods of using such compounds to treat or prevent diseases or disorders associated with the enzyme glycolate oxidase (GO). Such diseases or disorders include, for example, disorders of glyoxylate metabolism, including primary hyperoxaluria, that are associated with production of excessive amounts of oxalate.
Sequential Acetalization-Pyrolysis of α-Acetylcinnamates and α-Acetylbenzalacetones. A Method for the Generation of 2-Carbonyl-Subsituted Naphthalenes
Zoeller, Joseph R.,Sumner, Charles E.
, p. 319 - 324 (2007/10/02)
Substituted 2-acetonaphthones and 2-naphthoate methyl esters can be generated from benzaldehydes in a sequence of three reaction steps.Knoevenagel condensation of a benzaldehyde with 2,4-pentandione of methyl acetoacetate yields α-carbonyl-substituted benzalacetones.The α-carbonyl-substituted benzalacetones are then cyclized to generate the α-carbonyl-substituted naphthalenes by a sequential acetalization with trimethyl orthoformate followed by subsequent pyrolysis of the dimethyl acetal either in the vapor phase at 475 deg C or by being heated in boiling 1-methylnaphthalene. 2-Acetonaphthones are obtained when 2,4-pentanedione is used and 2-naphthoate methyl esters are obtained from methyl acetoacetate.
SEQUENTIAL ACETALIZATION-PYROLYSIS OF α-ACETYL BENZALACETONES. A METHOD FOR THE GENERATION OF 6-SUBSTITUTED 2-ACETONAPHTHONES
Zoeller, Joseph R.
, p. 1457 - 1460 (2007/10/02)
6-Substituted 2-acetonaphthones can be generated from para substituted benzaldehydes and acetylacetone (2,4-pentanedione) in three reactions consisting of condensing the benzaldehyde with acetylacetone, acetalizing the resultant 3-benzylidene 2,4-pentanedione (α-acetyl benzalacetones), with trimethyl orthoformate, pyrolyzing the acetal either in the vapor phase at 475 deg C or by heating in a high boiling solvent, such as 1-methylnaphthalene.
