-
1
-
-
0006551491
-
-
V. N. Kovtonyuk, A. Yu, Makarov, M. M. Shakirov, A. V. Zibarev, J. Chem. Soc. Chem. Commun., 1996, 1991.
-
(1996)
J. Chem. Soc. Chem. Commun.
, pp. 1991
-
-
Kovtonyuk, V.N.1
Makarov, A.Yu.2
Shakirov, M.M.3
Zibarev, A.V.4
-
2
-
-
0001123636
-
-
I. Yu. Bagryanskaya, H. Bock, Yu. V. Gatilov, A. Haas, M. M. Shakirov, B. Solouki, A. V. Zibarev, Chem. Ber. Recueil, 130, 1997, 247.
-
(1997)
Chem. Ber. Recueil
, vol.130
, pp. 247
-
-
Bagryanskaya, I.Yu.1
Bock, H.2
Gatilov, Yu.V.3
Haas, A.4
Shakirov, M.M.5
Solouki, B.6
Zibarev, A.V.7
-
3
-
-
0022601344
-
-
A. W. Cordes, M. Hojo, H. Koenig, M. C. Noble, R. T. Oakley, W. T. Pennington, Inorg. Chem., 25, 1986, 1137.
-
(1986)
Inorg. Chem.
, vol.25
, pp. 1137
-
-
Cordes, A.W.1
Hojo, M.2
Koenig, H.3
Noble, M.C.4
Oakley, R.T.5
Pennington, W.T.6
-
4
-
-
0001610978
-
-
A. V. Zibarev, Yu. V. Gatilov, A. O. Miller, Polyhedron, 11, 1992, 1137.
-
(1992)
Polyhedron
, vol.11
, pp. 1137
-
-
Zibarev, A.V.1
Gatilov, Yu.V.2
Miller, A.O.3
-
5
-
-
0004142484
-
-
Wiley Interscience, New York
-
V. I. Minkin, B. Ya. Simkin, M. N. Glukhovzev: Aromaticity and Antiaromaticity. Electronic and Structural Aspects, Wiley Interscience, New York (1994). For heterocyclic azathienes, see, for example, R. E. Hoffmeyer, W.-T. Chen, J. D. Goddard, R. T. Oakley, Can. J. Chem., 66, 1988, 2279.
-
(1994)
Aromaticity and Antiaromaticity. Electronic and Structural Aspects
-
-
Minkin, V.I.1
Simkin, B.Ya.2
Glukhovzev, M.N.3
-
6
-
-
6444223293
-
-
V. I. Minkin, B. Ya. Simkin, M. N. Glukhovzev: Aromaticity and Antiaromaticity. Electronic and Structural Aspects, Wiley Interscience, New York (1994). For heterocyclic azathienes, see, for example, R. E. Hoffmeyer, W.-T. Chen, J. D. Goddard, R. T. Oakley, Can. J. Chem., 66, 1988, 2279.
-
(1988)
Can. J. Chem.
, vol.66
, pp. 2279
-
-
Hoffmeyer, R.E.1
Chen, W.-T.2
Goddard, J.D.3
Oakley, R.T.4
-
7
-
-
0001176918
-
-
A. P. Hitchcock, R. S. DeWitte, J. M. Van Esbroek, P. Aebi, C. L. French, R. T. Oakley, N. P. C. Westwood, J. Electron Spectrosc. Relat. Phenom., 57, 1991, 165.
-
(1991)
J. Electron Spectrosc. Relat. Phenom.
, vol.57
, pp. 165
-
-
Hitchcock, A.P.1
Dewitte, R.S.2
Van Esbroek, J.M.3
Aebi, P.4
French, C.L.5
Oakley, R.T.6
Westwood, N.P.C.7
-
8
-
-
0000182382
-
-
N. E. Petrachenko, Yu. V. Gatilov, A. V. Zibarev, J. Electron Spectrosc. Relat. Phenom., 67, 1994, 489.
-
(1994)
J. Electron Spectrosc. Relat. Phenom.
, vol.67
, pp. 489
-
-
Petrachenko, N.E.1
Gatilov, Yu.V.2
Zibarev, A.V.3
-
9
-
-
0007312787
-
-
M. M. Shakirov, I. V. Beregovaya, A. V. Zibarev, Khim. Geterotsikl. Soedin., 1995, 262 (Chem. Abstr. 123, 1995, 55291j).
-
(1995)
Khim. Geterotsikl. Soedin.
, pp. 262
-
-
Shakirov, M.M.1
Beregovaya, I.V.2
Zibarev, A.V.3
-
10
-
-
33745346390
-
-
M. M. Shakirov, I. V. Beregovaya, A. V. Zibarev, Khim. Geterotsikl. Soedin., 1995, 262 (Chem. Abstr. 123, 1995, 55291j).
-
(1995)
Chem. Abstr.
, vol.123
-
-
-
11
-
-
37049070592
-
-
A. V. Zibarev, Yu. V. Gatilov, I. Yu. Bagryanskaya, A. M. Maksimov, A. O. Miller, J. Chem. Soc. Chem. Commun., 1993, 298.
-
(1993)
J. Chem. Soc. Chem. Commun.
, pp. 298
-
-
Zibarev, A.V.1
Gatilov, Yu.V.2
Bagryanskaya, I.Yu.3
Maksimov, A.M.4
Miller, A.O.5
-
13
-
-
0000001519
-
-
X.-G. Duan, X.-L. Duan, C. W. Rees, T.-Y. Yue, J. Heterocyclic Chem., 33, 1996, 1419.
-
(1996)
J. Heterocyclic Chem.
, vol.33
, pp. 1419
-
-
Duan, X.-G.1
Duan, X.-L.2
Rees, C.W.3
Yue, T.-Y.4
-
14
-
-
84986347631
-
-
A. V. Zibarev, A. O. Miller, Yu. V. Gatilov, G. G. Furin, Heteroatom Chem., 1, 1990, 443.
-
(1990)
Heteroatom Chem.
, vol.1
, pp. 443
-
-
Zibarev, A.V.1
Miller, A.O.2
Gatilov, Yu.V.3
Furin, G.G.4
-
15
-
-
85034563196
-
-
note
-
2o, only 17% (cf. also with Ref. [12]).
-
-
-
-
16
-
-
37049094190
-
-
H. W. Roesky, K.-L. Weber, U. Seseke, W. Pinkert, M. Noltemeyer, W. Clegg, G. M. Sheldrick, J. Chem. Soc. Dalton Trans., 1985, 565.
-
(1985)
J. Chem. Soc. Dalton Trans.
, pp. 565
-
-
Roesky, H.W.1
Weber, K.-L.2
Seseke, U.3
Pinkert, W.4
Noltemeyer, M.5
Clegg, W.6
Sheldrick, G.M.7
-
17
-
-
0003122847
-
-
T. Chivers, X. Gao, M. Parvez, Inorg. Chem., 35, 1996, 9.
-
(1996)
Inorg. Chem.
, vol.35
, pp. 9
-
-
Chivers, T.1
Gao, X.2
Parvez, M.3
-
20
-
-
0003422709
-
-
Wiley Interscience, New York
-
5R molecules; see Z. Zhou, R. G. Parr, J. Am. Chem. Soc., 112, 1990, 5720. The AH index is formulated in a Wheland-type late transition state approximation and takes its origin in the HSAB concept. The latter is known to encapsulate both thermodynamic and kinetic propensities of a molecules; see R. G. Pearson: Chemical Hardness, Wiley-VCH, New York (1997).
-
(1982)
Electrons in Chemical Reactions: First Principles
-
-
Salem, L.1
-
21
-
-
0013602932
-
-
5R molecules; see Z. Zhou, R. G. Parr, J. Am. Chem. Soc., 112, 1990, 5720. The AH index is formulated in a Wheland-type late transition state approximation and takes its origin in the HSAB concept. The latter is known to encapsulate both thermodynamic and kinetic propensities of a molecules; see R. G. Pearson: Chemical Hardness, Wiley-VCH, New York (1997).
-
(1990)
J. Am. Chem. Soc.
, vol.112
, pp. 5720
-
-
Zhou, Z.1
Parr, R.G.2
-
22
-
-
84949963475
-
-
Wiley-VCH, New York
-
5R molecules; see Z. Zhou, R. G. Parr, J. Am. Chem. Soc., 112, 1990, 5720. The AH index is formulated in a Wheland-type late transition state approximation and takes its origin in the HSAB concept. The latter is known to encapsulate both thermodynamic and kinetic propensities of a molecules; see R. G. Pearson: Chemical Hardness, Wiley-VCH, New York (1997).
-
(1997)
Chemical Hardness
-
-
Pearson, R.G.1
-
23
-
-
0000394005
-
-
I. Ernest, W. Holick, G. Rihs, D. Schomburg, G. Sholam, D. Wenkert, R. B. Woodward, J. Am. Chem. Soc., 103, 1981, 1540.
-
(1981)
J. Am. Chem. Soc.
, vol.103
, pp. 1540
-
-
Ernest, I.1
Holick, W.2
Rihs, G.3
Schomburg, D.4
Sholam, G.5
Wenkert, D.6
Woodward, R.B.7
-
24
-
-
0004062806
-
-
Wiley-Interscience, New York
-
J. K. Burdett: Molecular Shapes, Wiley-Interscience, New York (1980); see also, P. V. Schastnev, L. N. Shchegoleva: Molecular Distortions in Ionic and Excited States, CRC Press, Boca Raton, FL (1995).
-
(1980)
Molecular Shapes
-
-
Burdett, J.K.1
-
25
-
-
0004094438
-
-
CRC Press, Boca Raton, FL
-
J. K. Burdett: Molecular Shapes, Wiley-Interscience, New York (1980); see also, P. V. Schastnev, L. N. Shchegoleva: Molecular Distortions in Ionic and Excited States, CRC Press, Boca Raton, FL (1995).
-
(1995)
Molecular Distortions in Ionic and Excited States
-
-
Schastnev, P.V.1
Shchegoleva, L.N.2
-
26
-
-
0346460499
-
-
R. Gleiter, R. Bartetzko, D. Cremer, J. Am. Chem. Soc., 106, 1984, 437.
-
(1984)
J. Am. Chem. Soc.
, vol.106
, pp. 437
-
-
Gleiter, R.1
Bartetzko, R.2
Cremer, D.3
-
27
-
-
0000723569
-
-
I. Yu. Bagryanskaya, Yu. V. Gatilov, M. M. Shakirov, A. V. Zibarev, Zh. Stmkt. Khim., 37, 1996, 363 (Chem. Abstr., 126, 1997, 18931).
-
(1996)
Zh. Stmkt. Khim.
, vol.37
, pp. 363
-
-
Bagryanskaya, I.Yu.1
Gatilov, Yu.V.2
Shakirov, M.M.3
Zibarev, A.V.4
-
28
-
-
6444237224
-
-
I. Yu. Bagryanskaya, Yu. V. Gatilov, M. M. Shakirov, A. V. Zibarev, Zh. Stmkt. Khim., 37, 1996, 363 (Chem. Abstr., 126, 1997, 18931).
-
(1997)
Chem. Abstr.
, vol.126
, pp. 18931
-
-
-
29
-
-
84987491533
-
-
I. Yu. Bagryanskaya, Yu. V. Gatilov, A. O. Miller, M. M. Shakirov, A. V. Zibarev, Heteroatom Chem., 5, 1994, 561. The formation and ring opening of a spirocyclic intermediate can be considered as an example of unusual Smiles-type rearrangement; see G. M. Brooke, J. Fluor. Chem., 86, 1997, 1.
-
(1994)
Heteroatom Chem.
, vol.5
, pp. 561
-
-
Bagryanskaya, I.Yu.1
Gatilov, Yu.V.2
Miller, A.O.3
Shakirov, M.M.4
Zibarev, A.V.5
-
30
-
-
0031256513
-
-
I. Yu. Bagryanskaya, Yu. V. Gatilov, A. O. Miller, M. M. Shakirov, A. V. Zibarev, Heteroatom Chem., 5, 1994, 561. The formation and ring opening of a spirocyclic intermediate can be considered as an example of unusual Smiles-type rearrangement; see G. M. Brooke, J. Fluor. Chem., 86, 1997, 1.
-
(1997)
J. Fluor. Chem.
, vol.86
, pp. 1
-
-
Brooke, G.M.1
-
34
-
-
33947445466
-
-
R. Blatzly, M. Hanfenist, F. J. Webb, J. Am. Chem. Soc., 68, 1946, 2673.
-
(1946)
J. Am. Chem. Soc.
, vol.68
, pp. 2673
-
-
Blatzly, R.1
Hanfenist, M.2
Webb, F.J.3
-
38
-
-
0001414642
-
-
R. R. Gupta, K. G. Ojha, G. S. Kalvania, M. Kumar, Heterocycles, 14, 1980, 1145.
-
(1980)
Heterocycles
, vol.14
, pp. 1145
-
-
Gupta, R.R.1
Ojha, K.G.2
Kalvania, G.S.3
Kumar, M.4
-
40
-
-
0025967888
-
-
B. L. Mylari, E. R. Larson, T. A. Beyer, W. J. Zembrowski, C. E. Aldinger, M. F. Dee, T. W. Siegel, D. H. Singleton, J. Med. Chem., 34, 1991, 108.
-
(1991)
J. Med. Chem.
, vol.34
, pp. 108
-
-
Mylari, B.L.1
Larson, E.R.2
Beyer, T.A.3
Zembrowski, W.J.4
Aldinger, C.E.5
Dee, M.F.6
Siegel, T.W.7
Singleton, D.H.8
-
41
-
-
0006353731
-
-
M. R. Chedekel, D. E. Sharp, G. A. Jeffery, Synth. Commun., 10, 1980, 167.
-
(1980)
Synth. Commun.
, vol.10
, pp. 167
-
-
Chedekel, M.R.1
Sharp, D.E.2
Jeffery, G.A.3
-
42
-
-
0000974662
-
-
A. V. Zibarev, A. O. Miller, J. Fluor. Chem., 50, 1990, 359. For an additional example, see reduction of 54 to 55 (Scheme 4 and Experimental).
-
(1990)
J. Fluor. Chem.
, vol.50
, pp. 359
-
-
Zibarev, A.V.1
Miller, A.O.2
-
43
-
-
0002990550
-
-
F. H. Allen, O. Kennard, D. G. Watson, L. Brammer, A. G. Orpen, R. Taylor, J. Chem. Soc. Perkin Trans. II, 1987, 51.
-
(1987)
J. Chem. Soc. Perkin Trans. II
, pp. 51
-
-
Allen, F.H.1
Kennard, O.2
Watson, D.G.3
Brammer, L.4
Orpen, A.G.5
Taylor, R.6
-
44
-
-
85034532600
-
-
Specialized fund of quantum chemical programs of the Siberian Division of the Russian Academy of Sciences. Institute of Chemical Kinetics and Combustion, Novosibirsk, Russia
-
Specialized fund of quantum chemical programs of the Siberian Division of the Russian Academy of Sciences. Institute of Chemical Kinetics and Combustion, Novosibirsk, Russia.
-
-
-
-
45
-
-
84943920280
-
-
G. Kresze, A. Maschke, R. Albrecht, K. Bederke, H. P. Patzchke, H. Smalla, A. Trede, Angew. Chem. Int. Ed. Engl, 1, 1962, 89.
-
(1962)
Angew. Chem. Int. Ed. Engl
, vol.1
, pp. 89
-
-
Kresze, G.1
Maschke, A.2
Albrecht, R.3
Bederke, K.4
Patzchke, H.P.5
Smalla, H.6
Trede, A.7
-
47
-
-
37049122435
-
-
R. E. Banks, R. N. Haszeldine, D. R. Karsa, F. E. Pickett, I. M. Young, J. Chem. Soc., C, 1969, 1660.
-
(1969)
J. Chem. Soc., C
, pp. 1660
-
-
Banks, R.E.1
Haszeldine, R.N.2
Karsa, D.R.3
Pickett, F.E.4
Young, I.M.5
-
48
-
-
85013564019
-
-
Netherlands Patent 6 516 406 (1966)
-
Netherlands Patent 6 516 406 (1966) (Chem. Abstr., 65, 1966, 18564e).
-
(1966)
Chem. Abstr.
, vol.65
-
-
-
49
-
-
37049064236
-
-
R. E. Banks, J. F. Burgess, W. M. Cheng, R. N. Haszeldine, J. Chem. Soc., 1965, 575.
-
(1965)
J. Chem. Soc.
, pp. 575
-
-
Banks, R.E.1
Burgess, J.F.2
Cheng, W.M.3
Haszeldine, R.N.4
-
50
-
-
0002511555
-
-
Chambers, J. Hutchinson, W. K. R. Masgrave, J. Chem. Soc., 1964, suppl. 1, 5634.
-
(1964)
J. Chem. Soc.
, Issue.SUPPL. 1
, pp. 5634
-
-
Chambers1
Hutchinson, J.2
Masgrave, W.K.R.3
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