Kinetics and Mechanism of the Pudovik Reaction in the Series of Shiff Bases. Addition of Dialkylphosphites to Substituted N-Alkyl(Aryl)Benzylideneamines

1999 ◽  
Vol 147 (1) ◽  
pp. 71-71
Author(s):  
A. A. Sobanov ◽  
A. V. Zolotukhin ◽  
V. I. Galkin ◽  
I. V. Galkina ◽  
R. A. Cherkasov
2006 ◽  
Vol 76 (3) ◽  
pp. 421-429 ◽  
Author(s):  
A. A. Sobanov ◽  
A. V. Zolotukhin ◽  
I. V. Galkina ◽  
V. I. Galkin ◽  
R. A. Cherkasov

1990 ◽  
Vol 49-50 (1-4) ◽  
pp. 61-64 ◽  
Author(s):  
R. A. Cherkasov ◽  
V. I. Galkin ◽  
A. B. Khabibullina ◽  
Khalil Al Kurdi

2004 ◽  
pp. 1
Author(s):  
T. Ooi ◽  
K. Maruoka

2007 ◽  
Vol 20 (4) ◽  
pp. 255-263 ◽  
Author(s):  
Arunachalam Chellamani ◽  
Nainamohamed Ismail Alhaji ◽  
Seenivasan Rajagopal

1997 ◽  
Vol 62 (8) ◽  
pp. 2512-2517 ◽  
Author(s):  
Enrique A. Castro ◽  
María Cubillos ◽  
José G. Santos ◽  
Jimena Téllez

2019 ◽  
Vol 194 (4-6) ◽  
pp. 463-466 ◽  
Author(s):  
Irina V. Galkina ◽  
Khasan R. Khayarov ◽  
Rustam R. Davletshin ◽  
Aynaz Z. Gaynullin ◽  
Alexander V. Gerasimov ◽  
...  

2017 ◽  
Vol 6 (2) ◽  
Author(s):  
György Keglevich ◽  
Zita Rádai ◽  
Nóra Zsuzsa Kiss

AbstractRecent synthetic methods for α-hydroxyphosphonates comprise a green, solvent-free accomplishment of the Pudovik reaction that was typically followed by extractions and recrystallization, or even by chromatography, or other operations. We now developed a general procedure applying 10% of triethylamine as the catalyst and a minimum quantity of acetone as the solvent, giving the products in a pure form after a reflux of 5–120 min following the addition of some


2015 ◽  
Vol 13 (1) ◽  
pp. 132-141 ◽  
Author(s):  
Alexey V. Salin ◽  
Anton V. Il';in ◽  
Fanuza G. Shamsutdinova ◽  
Albert R. Fatkhutdinov ◽  
Daut R. Islamov ◽  
...  

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