5044-62-2Relevant academic research and scientific papers
Ketones in the catalytic three-component "one-pot" Kabachnik - Fields synthesis of α-amino phosphonates
Matveeva,Podrugina,Prisyajnoy,Zefirov
, p. 1209 - 1214 (2006)
Reactions of carbocyclic, heterocyclic, and steroidal ketones with benzylamine and diethyl phosphite in a catalytic three-component "one-pot" synthesis of α-amino phosphonates were studied. The activities of mono-and binuclear complexes of tetra(tert-butyl)phthalocyanines as catalysts for this process were compared. Springer Science+Business Media, Inc. 2006.
ORGANOPHOSPHORUS CHEMISTRY, 27. THE REACTION OF ISATIN, 5-METHYLISATIN AND THEIR MONOXIMES WITH ALKYL PHOSPHITES, TRIPHENYLPHOSPHINE AND PHOSPHORUS YLIDES
Mahran, M. R. H.,Khidre, M. D.,Abdou, W. M.
, p. 17 - 28 (2007/10/02)
5-Methylisatin (1b) reacts with TAP (4a-c) and/or DAP (3a-c) to give the respective dialkyl α-hydroxyphosphonates (8a-c).Isatin-monoxime (5a) and 5-methyl isatin-monoxime (5b) react with alkyl phosphites to give dialkyl 2-oxo-indolyl phosphonates (8a-c, 12a-f, 15a-c) as major products.The carbonyl-group at position - 3 in 1b is deoxygenated by triphenylphosphine to give a new phosphorus ylide (17) and by methylenetriphenylphosphoranes (Wittig-reagents, 7a-c) to afford the respective 3-substituted methylenes (19a-c) in good yields.Possible reaction mechanisms were considered and structural assignments were based upon analytical, chemical and spectroscopic (IR, 1H NMR, 31P NMR and MS) results. Key words: Isatins, isatinmonoximes, phosphorylation, triphenylphsophine, Wittig-reaction.
