106881-77-0Relevant articles and documents
Unusual course of the p-nitrophenyl phosphate esters cleavage by 3-hydroxyiminoalkylpyridinium salts in micellar solutions
Kotoucova, Hana,Mazac, Jiri,Cibulka, Radek,Hampl, Frantisek,Liska, Frantisek
, p. 649 - 650 (1998)
Two types of amphiphilic quaternary 3-pyridinium ketoximes with different position of the hydrophobic alkyl chain were synthesized and tested as hydrolytic micellar catalysts. A considerable positive deviation from the expected first-order curve was observed in the absorbance vs time plot when p-nitrophenyl diphenyl phosphate and p-nitrophenyl diethyl phosphate were hydrolyzed in micellar solutions of the prepared ketoximes under pseudo-first-order reaction conditions.
Stereospecific synthesis of 1,5-disubstituted tetrazoles from ketoximes via a Beckmann rearrangement facilitated by diphenyl phosphorazidate
Ishihara, Kotaro,Shioiri, Takayuki,Matsugi, Masato
supporting information, p. 1295 - 1298 (2019/04/13)
A novel method for the stereospecific synthesis of 1,5-disubstituted tetrazoles from ketoximes via the Beckmann rearrangement was developed using diphenyl phosphorazidate (DPPA) as both the oxime activator and azide source. Various ketoximes were transformed into the corresponding 1,5-disubstituted tetrazoles with exclusive trans-group migration and no E-Z isomerization of the ketoxime. This method enables the preparation of 1,5-disubstituted tetrazoles without using toxic or explosive azidation reagents.
Modulation of PPAR subtype selectivity. Part 2: Transforming PPARα/γ dual agonist into α selective PPAR agonist through bioisosteric modification
Zaware, Pandurang,Shah, Shailesh R.,Pingali, Harikishore,Makadia, Pankaj,Thube, Baban,Pola, Suresh,Patel, Darshit,Priyadarshini, Priyanka,Suthar, Dinesh,Shah, Maanan,Jamili, Jeevankumar,Sairam, Kalapatapu V.V.M.,Giri, Suresh,Patel, Lala,Patel, Harilal,Sudani, Hareshkumar,Patel, Hiren,Jain, Mukul,Patel, Pankaj,Bahekar, Rajesh
scheme or table, p. 628 - 632 (2011/03/18)
A novel series of oxime containing benzyl-1,3-dioxane-r-2-carboxylic acid derivatives (6a-k) were designed as selective PPARα agonists, through bioisosteric modification in the lipophilic tail region of PPARα/γ dual agonist. Some of the test compounds (6a
Catalytic enantioselective borane reduction of benzyl oximes: Preparation of (S)-1-pyridin-3-YL-ethylamine bis hydrochloride
Huang, Kun,Ortiz-Marciales, Margarita,Hughes, David
experimental part, p. 36 - 52 (2011/05/13)
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