Эта публикация цитируется в 13 научных статьях (всего в 13 статьях)
An alternative reaction of ortho-(N-benzylidene)aminophenol with chlorophosphites: formation of 2-(2’-alkoxy)-2-oxo-3-phenyl-5,6-benzo-1,4,2-oxazaphosphorinanes
Аннотация:
The reactions of o-(N-benzylidene)aminophenol with ethylene chlorophosphite and diethyl chlorophosphite in CHCl3 in the absence of an external acceptor of HCl result in the formation of diastereomeric 2-(2’-alkoxy)-2-oxo-3-phenyl-5,6-benzo-1,4,2-oxazaphosphorinanes different in the configurations of phosphorus atoms.
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
M. N. Dimukhametov, E. V. Bayandina, E. Yu. Davydova, A. B. Dobrynin, A. T. Gubaidullin, I. A. Litvinov, V. A. Alfonsov, “An alternative reaction of ortho-(N-benzylidene)aminophenol with chlorophosphites: formation of 2-(2’-alkoxy)-2-oxo-3-phenyl-5,6-benzo-1,4,2-oxazaphosphorinanes”, Mendeleev Commun., 11:5 (2001), 196–197
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc4290
https://www.mathnet.ru/rus/mendc/v11/i5/p196
Эта публикация цитируется в следующих 13 статьяx:
K. E. Metlushka, R. G. Zinnatullin, K. A. Nikitina, E. K. Badeeva, “Chiral 2-Oxo-1,4,2-oxazaphosphorinanes: Synthesis, Structure, and Applications (A Review)”, Russ J Gen Chem, 93:9 (2023), 2237
K. E. Metlushka, R. G. Zinnatullin, K. A. Nikitina, E. K. Badeeva, “Chiral 2-oxo-1,4,2-oxazaphosphorinanes: synthesis, structure and applications (a review)”, Žurnal obŝej himii, 93:9 (2023), 1365
Abgeena Shabir, Abid, Poonam Sehrawat, C M Julien, S S Islam, “Reversible synthesis of GO: Role of differential bond structure transformation in fine-tuning photodetector response”, Nanotechnology, 32:4 (2021), 045601
K. E. Metlushka, D. N. Sadkova, K. A. Nikitina, Z. R. Yamaleeva, K. A. Ivshin, O. N. Kataeva, V. A. Alfonsov, “A new synthetic route to chiral 3-aryl-5-ethyl-1,4,2-oxazaphosphorines”, Mendeleev Commun., 28:6 (2018), 579–581
Mounir A. I. Salem, Tarik E. Ali, Magda I. Marzouk, “Electron Ionization Mass Spectra of Organophosphorus Compounds Part I: The Mass Fragmentation Pathways of Cyclic α-Aminophosphonates Monoester Containing 1,2,4-Triazinone Moiety”, Phosphorus, Sulfur, and Silicon and the Related Elements, 187:3 (2012), 336
Marina Juribašić, Lisa Bellotto, Ljerka Tušek-Božić, “N–H···O=P hydrogen-bonded dimers as the main structural motif of aminophosphonate diesters”, Struct Chem, 23:1 (2012), 257
M. N. Dimukhametov, L. M. Abdrakhmanova, V. F. Mironov, R. Z. Musin, “Intramolecular transformation of 2-benzylideneaminoethoxybenzo[d]-1,3,2-dioxaphosphorin-4-one into 3,4-benzo-10-phenyl-1-aza-5,7-dioxa-6-phosphabicyclo-[4.3.1]decane-2,6-dione”, Russ J Gen Chem, 80:10 (2010), 2073
M. N. Dimukhametov, V. F. Mironov, R. Z. Musin, “Formation of 2,7-dioxa-5,10-diaza-3,8-diphospha-1,6(1,4)-dibenzenacyclodecaphane derivatives in the reactions of para-(N-benzylidene)aminophenol with monochlorophosphites”, Mendeleev Commun., 16:1 (2006), 48–50
C.S. Kenesky, G.A. Molander, Comprehensive Organic Functional Group Transformations II, 2005, 443
P. I. Gryaznov, O. E. Naumova, D. R. Alimova, D. B. Krivolapov, I. A. Litvinov, V. A. Al'fonsov, “Reaction of Lawesson Reagent with 1,2-(N-Benzyliden)iminoalcohols”, Russ J Gen Chem, 75:11 (2005), 1744
Eric J. Stoner, Peter P. Giannousis, Lisheng Cai, Encyclopedia of Reagents for Organic Synthesis, 2004
M. N. Dimukhametov, M. A. Abaskalova, E. Yu. Davydova, E. V. Bayandina, A. B. Dobrynin, I. A. Litvinov, V. A. Alfonsov, “Reactions of sodium N-benzylideneglycinate with dialkyl chlorophosphites: formation of 1,4-bis[α-(dialkoxyphosphoryl)benzyl]piperazine-2,5-diones”, Mendeleev Commun., 14:1 (2004), 35–37
Mudaris N. Dimukhametov, Eugenia V. Bajandina, Elena Yu. Davydova, Alexey B. Dobrynin, Aidar T. Gubaidullin, Igor A. Litvinov, Vladimir A. Alfonsov, “ChemInform Abstract: An Alternative Reaction of ortho‐(N‐Benzylidene)aminophenol with Chlorophosphites: Formation of 2‐(2′‐Alkoxy)‐2‐oxo‐3‐phenyl‐5,6‐benzo‐1,4,2‐oxazaphosphorinanes.”, ChemInform, 33:11 (2002)
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