220901-47-3Relevant academic research and scientific papers
Efficient Microwave Method for the Oxidative Coupling of Phenols
Grant-Overton, Sharday,Buss, Joshua A.,Smith, Eva H.,Gutierrez, Elisa G.,Moorhead, Eric J.,Lin, Vivian S.,Wenzel, Anna G.
, p. 331 - 337 (2015)
The tert-butyl peroxide-initiated, oxidative coupling of phenols can frequently promote reactions that otherwise perform poorly under alternative conditions. Despite this utility, peroxide coupling reactions employing conventional heat often require high-
2- ( 2 -HYDROXYPHENYL) -QUINAZOLIN-4-ONES USEFUL FOR TREATING OBESITY AND DIABETES
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Page/Page column 14, (2010/10/19)
The present invention relates to novel compounds that act as chemical uncouplers. Compounds of the invention are useful, inter alia, in the treatment, including prevention, of obesity, diabetes and a number of diseases or conditions associated therewith.
Electron-withdrawing, bipheny 1-2,2 -diol-based compounds for asymmetric catalysis
Gutierrez, Elisa G.,Moorhead, Eric J.,Smith, Eva H.,Lin, Vivian,Ackerman, Laura K. G.,Knezevic, Claire E.,Sun, Victoria,Grant, Sharday,Wenzel, Anna G.
experimental part, p. 3027 - 3031 (2010/08/07)
Facile synthetic routes to a chiral chloro-substituted biphenyl-2,2′- diyl hydrogen phosphate and a chiral O,O-biphenyl-2,2′-diyl phosphoramidothioate are described. The performance of these compounds as catalysts for the hydrophosphorylation of imines and the Friedel-Crafts alkylation of indole was investigated. In the latter reaction, the chlorosubstituted phosphoric acid derivative was found to rival the best Bronsted acid catalysts reported to date.
2- ( 2 -HYDROXYPHENYL) -QUINAZOLIN-4-ONES USEFUL FOR TREATING OBESITY AND DIABETES
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Page/Page column 39-40, (2008/12/05)
The present invention relates to novel compounds that act as chemical uncouplers. Compounds of the invention are useful, inter alia, in the treatment, including prevention, of obesity, diabetes and a number of diseases or conditions associated therewith.
C (2) -HETEROARYLMETHYL-C (4) -METHOXYMETHYL ACYL PYRROLIDINE COMPOUNDS AND THEIR USE FOR TREATING VIRAL INFECTIONS, ESPECIALLY HEPATITIS C VIRUS
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Page/Page column 32, (2010/11/26)
Anti-viral agents of Formula (Ia): wherein A represents hydroxyl; D represents 4-tert-butyl-3-ethenylphenyl or 4-tert-butyl-5-ethenyl-2-fluorophenyl; E represents 1,3-thiazol-2-yl; G represents methoxymethyl; J represents 1,3-thiazol-4-ylmethyl or 1H-pyra
C (2) -HETEROARYLMETHYL-C (4) -PYRAZIN-2-YL ACYL PYRROLIDINE COMPOUNDS AND THEIR USER FOR TREATING VIRAL INFECTIONS, ESPECIALLY HEPATITICS C (HCV)
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Page/Page column 27, (2010/11/26)
Anti-viral agents of Formula (Ia) : wherein A represents hydroxy; B represents -C(O)R3; D represents 1,3-thiazol-2-yl; E represents pyrazin-2-yl; G represents 1,3-thiazol-4-ylmethyl or 1H-pyrazol-1-ylmethyl; R3 represents 4-tert-buty
PYRROLIDINE DERIVATIVES FOR TREATING VIRAL INFECTIONS
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Page/Page column 29, (2010/11/26)
Anti-viral agents of Formula (Ia): wherein A represents hydroxy; D represents 3-bromo-4-tert-butylphenyl or 5-bromo-4-tert-butyl-2-fluorophenyl; E represents 1,3-thiazol-2-yl or 5-methylisoxazol-3-yl; G represents methoxymethyl; J represents 1,3-thiazol-4
C (2) -HETEROARYLMETHYL-C (4) -PYRAZINYL-2-YL ACYL PYRROLIDINE COMPOUNDS AND THEIR USE FOR TREATING VIRAL INFECTIONS, ESPECIALLY HEPATITIS C VIRUS
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Page/Page column 23, (2010/11/26)
Anti-viral agents of Formula (Ia) : wherein A represents hydroxy; B represents -C(O)R3; D represents 1,3-thiazol-2-yl or 5-methylisoxazol-3-yl; E represents pyrazin-2-yl; G represents 1,3-thiazol-4-ylmethyl or 1H-pyrazol-1-ylmethyl; R3 /s
