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Catalytic synthesis and transformations of organophosphorus compounds

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Beletskaya I. P., Kabachnik M. M. Catalytic synthesis and transformations of organophosphorus compounds // Mendeleev Communications. 2008. Vol. 18. No. 3. pp. 113-120.
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Beletskaya I. P., Kabachnik M. M. Catalytic synthesis and transformations of organophosphorus compounds // Mendeleev Communications. 2008. Vol. 18. No. 3. pp. 113-120.
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TY - JOUR
DO - 10.1016/j.mencom.2008.05.001
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2008.05.001
TI - Catalytic synthesis and transformations of organophosphorus compounds
T2 - Mendeleev Communications
AU - Beletskaya, Irina Petrovna
AU - Kabachnik, Mariya Martinovna
PY - 2008
DA - 2008/05/14
PB - Mendeleev Communications
SP - 113-120
IS - 3
VL - 18
ER -
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@article{2008_Beletskaya,
author = {Irina Petrovna Beletskaya and Mariya Martinovna Kabachnik},
title = {Catalytic synthesis and transformations of organophosphorus compounds},
journal = {Mendeleev Communications},
year = {2008},
volume = {18},
publisher = {Mendeleev Communications},
month = {May},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2008.05.001},
number = {3},
pages = {113--120},
doi = {10.1016/j.mencom.2008.05.001}
}
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Beletskaya, Irina Petrovna, and Mariya Martinovna Kabachnik. “Catalytic synthesis and transformations of organophosphorus compounds.” Mendeleev Communications, vol. 18, no. 3, May. 2008, pp. 113-120. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2008.05.001.
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Abstract

Methods for the catalytic synthesis of organophosphorus compounds with three- and four-coordinate phosphorus and their transformations are summarised. Special attention is given to the synthesis of aryl(vinyl)-substituted phosphonates and phosphinates, as well as aminophosphonates, which are of particular interest due to their high biological activity.

References

1.
I. P. Beletskaya, in Chemical Weapon Destruction in Russia: Political, Legal and Technical Aspects, eds. J. Hart and C. D. Miller, SIPRI Chemical & Biological Warfare Studies, no. 17, Oxford University Press, Oxford, New York, 1998, p. 103.
2.
10.1016/j.mencom.2008.05.001_bib2
Uziel
Zh. Org. Khim, 1997
3.
N. M. Dyatlova, V. Ya. Temkina and K. I. Popov, Kompleksony i kompleksonaty metallov (Metal Complexones and Complexonates), Khimiya, Moscow, 1988, p. 544.(in Russian).
4.
Poly (diphenylphosphinomethyl)benzene oxides ? New organophosphorus extractants
Bodrin G.V., Kabachnik M.I., Kochetkova N.E., Medved' T.Y., Myasoedov B.F., Polikarpov Y.M., Chmutova M.K.
Russian Chemical Bulletin, 1979
5.
S. A. Pisareva, F. I. Bel'skii, T. Ya. Medved’ and M. I. Kabachnik, Izv. Akad. Nauk, Ser. Khim., 1987, 413.(Bull. Acad. Sci. USSR, Div. Chem. Sci., 1987, 36, 372).
8.
Catalytic Carbonylation Reactions
Topics in Organometallic Chemistry, 2006
9.
10.1016/j.mencom.2008.05.001_bib9_1
Weil
Flame Retardant Polymeric Materials, 1979
10.
10.1016/j.mencom.2008.05.001_bib9_2
Stelzer
Top. Phosphorus Chem., 1977
11.
10.1016/j.mencom.2008.05.001_bib10
Kabachnik
Zh. Obshch. Khim., 1979
12.
Synthesis and some properties of phosphorus-substituted azomethines
Kabachnik M.M., Novikova Z.S., Chadnaya I.A., Borisenko A.A., Beletskaya I.P.
Russian Chemical Bulletin, 1998
13.
10.1016/j.mencom.2008.05.001_bib12
Novikova
Zh. Org. Khim., 1993
15.
A. D. Averin, N. V. Lukashev, M. A. Kazankova and I. P. Beletskaya, Mendeleev Commun., 1993, 69.
16.
10.1016/j.mencom.2008.05.001_bib15
Averin
Zh. Org. Khim., 2002
17.
10.1016/j.mencom.2008.05.001_bib16
Averin
Zh. Org. Khim., 2000
18.
10.1016/j.mencom.2008.05.001_bib17
Averin
Zh. Obshch. Khim., 1998
19.
10.1016/j.mencom.2008.05.001_bib18
Averin
Zh. Org. Khim., 1996
20.
10.1016/j.mencom.2008.05.001_bib19
Lukashev
Phosphorus Sulfur Silicon Relat. Elem., 1996
21.
10.1016/j.mencom.2008.05.001_bib20
Averin
Zh. Org. Khim., 1995
22.
10.1016/j.mencom.2008.05.001_bib21
Averin
Zh. Org. Khim., 1995
23.
10.1016/j.mencom.2008.05.001_bib22
Arbuzov
J. Russ. Phys. Chem. Soc., 1906
24.
Michaelis-Arbusow- und Perkow-Reaktionen
Arbusow B.A.
Pure and Applied Chemistry, 1964
25.
Michaelis-Arbuzov rearrangement
Bhattacharya A.K., Thyagarajan G.
Chemical Reviews, 1981
27.
Synthesis of cinnamylphosphonates
Demik N.N., Kabachnik M.M., Novikova Z.S., Beletskaya I.P.
Russian Chemical Bulletin, 1992
28.
10.1016/j.mencom.2008.05.001_bib27
Kazankova
Zh. Org. Khim., 1999
29.
Nickel- and palladium-catalyzed cross-coupling as a route to 1- and 2- alkoxy- or dialkylaminovinylphosphonates
Kazankova M.A., Trostyanskaya I.G., Lutsenko S.V., Beletskaya I.P.
Tetrahedron Letters, 1999
30.
Cross-coupling of E,E-1,4-diiodobuta-1,3-diene with nucleophiles catalyzed by Pd or Ni complexes: A new route to functionalized dienes
Trostyanskaya I.G., Titskiy D.Y., Anufrieva E.A., Borisenko A.A., Kazankova M.A., Beletskaya I.P.
Russian Chemical Bulletin, 2001
31.
A Novel Synthesis of Dialkyl Arenephosphonates
Hirao T., Masunaga T., Ohshiro Y., Agawa T.
Synthesis, 1981
32.
Palladium-catalyzed New Carbon-Phosphorus Bond Formation
Hirao T., Masunaga T., Yamada N., Ohshiro Y., Agawa T.
Bulletin of the Chemical Society of Japan, 1982
33.
Palladium-catalyzed alkylations in aqueous media
Casalnuovo A.L., Calabrese J.C.
Journal of the American Chemical Society, 1990
34.
10.1016/j.mencom.2008.05.001_bib33
Kabachnik
Zh. Org. Khim., 1998
36.
Stereoselective synthesis of vinylphosphonate
Hirao T., Masunaga T., Ohshiro Y., Agawa T.
Tetrahedron Letters, 1980
37.
I. P. Beletskaya, E. A. Chirkov, D. Yu. Titskyi, I. G. Trostyanskaya and M. A. Kazankova, Book of Abstracts of XX International Conference on Organometallic Chemistry, Corfu, 2002, p. 214.
39.
10.1016/j.mencom.2008.05.001_bib38
Beletskaya
Zh. Org. Khim., 2006
40.
10.1016/j.mencom.2008.05.001_bib39
Beletskaya
Zh. Org. Khim., 2004
43.
10.1016/j.mencom.2008.05.001_bib41_1
Beletskaya
Izv. Akad. Nauk, Ser. Khim., 1992
44.
10.1016/j.mencom.2008.05.001_bib41_2
Veits
Zh. Org. Khim., 1998
45.
Synthesis of vinyldiphenylphosphines of Pd-catalyzed cross-coupling reactions of diphenylphosphine with alkenylhalides
Kazankova M.A., Chirkov E.A., Kochetkov A.N., Efimova I.V., Beletskaya I.P.
Tetrahedron Letters, 1999
46.
New Approach to Phosphinoalkynes Based on Pd- and Ni-Catalyzed Cross-Coupling of Terminal Alkynes with Chlorophosphanes
47.
A Convenient and Direct Route to Phosphinoalkynes via Copper-Catalyzed Cross-Coupling of Terminal Alkynes with Chlorophosphanes
48.
10.1016/j.mencom.2008.05.001_bib45
Beletskaya
Zh. Org. Khim., 2002
50.
Catalytic Asymmetric Synthesis of .alpha.-Amino Phosphonates Using Lanthanoid-Potassium-BINOL Complexes
52.
New approach to vinylphosphines based on Pd- and Ni-catalyzed diphenylphosphine addition to alkynes
Kazankova M.A., Efimova I.V., Kochetkov A.N., Afanas'ev V.V., Beletskaya I.P., Dixneuf P.H.
Synlett, 2001
54.
Catalytic hydrophosphination of styrenes
Shulyupin M.O., Kazankova M.A., Beletskaya I.P.
Organic Letters, 2002
55.
10.1016/j.mencom.2008.05.001_bib51
Gulyukina
Zh. Org. Khim., 2003
56.
Regio- and enantioselective catalytic hydrophosphorylation of vinylarenes
Shulyupin M., Franciò G., Beletskaya I., Leitner W.
Advanced Synthesis and Catalysis, 2005
57.
10.1016/j.mencom.2008.05.001_bib53
Kabachnik
Zh. Org. Khim., 2005
58.
First synthesis of α-aminophosphonates from natural porphyrin derivatives by the Kabachnik - Fields reaction
Kabachnic M.M., Zobnina E.V., Pavlov V.Y., Konstantinov I.O., Ponomarev G.V., Beletskaya I.P.
Russian Chemical Bulletin, 2005
60.
M. M. Kabachnik, E. V. Zobnina and I. P. Beletskaya, Phosphorus Sulfur Silicon Relat. Elem., 2008.(in press).
61.
10.1016/j.mencom.2008.05.001_bib57
Bellucci
Farmaco, 1989
62.
Syntheses and biological evaluation of two new naproxen analogs
Kyung Woon Jung, Janda K.D., Sanfilippo P.J., Wachter M.
Bioorganic and Medicinal Chemistry Letters, 1996
63.
P. Kafarski, in Aminophosphonic and Aminophosphinic Acids. Chemistry and Biological Activity, eds. H. R. Hudson and V. P. Kukhar, Wiley, New York, 2002, p. 634.
64.
10.1016/j.mencom.2008.05.001_bib60
Finashina
Zh. Org. Khim., 2006
65.
A practical synthetic approach to chiral α-aryl substituted ethylphosphonates
Goulioukina N.S., Dolgina T.M., Beletskaya I.P., Henry J., Lavergne D., Ratovelomanana-Vidal V., Genet J.
Tetrahedron Asymmetry, 2001
66.
Highly enantioselective hydrogenation of α,β-unsaturated phosphonates with iridium-phosphinooxazoline complex: Synthesis of a phosphorus analogue of naproxen
Goulioukina N.S., Dolgina T.M., Bondarenko G.N., Beletskaya I.P., Ilyin M.M., Davankov V.A., Pfaltz A.
Tetrahedron Asymmetry, 2003
67.
10.1016/j.mencom.2008.05.001_bib63
Bondarenko
Khim. Farm. Zh., 2003
68.
I. D. Gridnev, M. Yasutake, T. Imamoto and I. P. Beletskaya, Proceedings of the National Academy of Sciences of the USA, 2004, 101, 5385.
69.
10.1016/j.mencom.2008.05.001_bib65
Gulyukina
Zh. Org. Khim., 2007
70.
Catalytic hydrogenation of α-iminophosphonates as a method for the synthesis of racemic and optically active α-aminophosphonates
Goulioukina N., Bondarenko G., Lyubimov S., Davankov V., Gavrilov K., Beletskaya I.
Advanced Synthesis and Catalysis, 2008
71.
Trifluoromethylated cyclopropanes and epoxides from CuI-mediated transformations of α-trifluoromethyl-diazophosphonate
72.
10.1016/j.mencom.2008.05.001_bib68
Titanyuk
Synlett, 2006