98293-46-0Relevant academic research and scientific papers
Cyclocondensation reactions of heterocyclic carbonyl compounds XI [1]. Synthesis and study of cyclocondensation reactions of some 3-substituted-5-(2- aminobenzyl)-1H-[1,2,4]triazine-6-ones
Gucky, Tomas,Slouka, Jan,Malon, Michal,Frysova, Iveta
, p. 613 - 621 (2007/10/03)
A series of 2-substituted-4-(2-nitrobenzylidene)-4,5-dihydrooxazol-5-ones (2a-2i) was prepared by the Erlenmeyer's synthesis of 2-nitrobenzaldehyde with acylglycines (1a-1i) and the series of corresponding aminoderivatives (3b-3d and 3g-3i) was synthetise
Deracemisation of aryl substituted α-hydroxy esters using Candida parapsilosis ATCC 7330: Effect of substrate structure and mechanism
Baskar,Pandian,Priya,Chadha, Anju
, p. 12296 - 12306 (2007/10/03)
Candida parapsilosis ATCC 7330 was found to be an efficient biocatalyst for the deracemisation of aryl α-hydroxy esters (65-85% yield and 90-99% ee). A variety of aryl and aryl substituted α-hydroxy esters were synthesized to reflect steric and electronic effects on biocatalytic deracemisation. The mechanism of this biocatalytic deracemisation was found to be stereoinversion.
2-METHYL-4-(o-NITROBENZYLIDENE)OXAZOL-5-ONES
Mazurov, A. A.,Andronati, S. A.,Antonenko, V. V.
, p. 514 - 515 (2007/10/02)
The cis and trans isomers of 2-methyl-4-(o-nitrobenzylidene)oxazol-5-one have been obtained.On reduction, the cis isomer formed 3-acetamidoquinolin-2-ol, and the trans isomer formed 4-(o-aminobenzylidene)-2-methyloxazol-5-one.Details of the IR, UV, PMR, a
