anisotropic approximation for 2457 reflections for non-hydrogen atoms were taken to wR2 = 0.118 (R1 = 0.049
for 1505 reflections with F > 4σ(F), S = 0.97). Full crystallographic data has been deposited with the Cambridge
structural database (deposit CCDC 283294).
The authors thank the National Institute for Allergy and Infections Diseases of the USA for the study of
the antitubercular properties of the compounds synthesized by us (contract No. 01-A1-45246).
REFERENCES
1.
2.
3.
4.
I. V. Ukrainets, L. V. Sidorenko, O. V. Gorokhova, N. L. Bereznyakova, and S. V. Shishkina, Khim.
Geterotsikl. Soedin., 1502 (2006). [Chem. Heterocycl. Comp., 42, 1296 (2006)].
I. V. Ukrainets, S. G. Taran, P. A. Bezuglyi, S. N. Kovalenko, A. V. Turov, and N. A. Marusenko, Khim.
Geterotsikl. Soedin., 1223 (1993). [Chem. Heterocycl. Comp., 29, 1044 (1993)].
I. V. Ukrainets, A. Kh. N. Dakkakh, S. G. Taran, O. V. Gorokhova, L. V. Sidorenko, and S. G. Leonova,
Physiologically Active Substances [in Russian], No. 1 (29), 18 (2000).
I. V. Ukrainets. A. Kh. N. Dakkakh, P. A. Bezuglyi, O. V. Gorokhova, L. V. Sidorenko, and
T. V. Alekseeva, Vestnik Farmatsii, No. 1 (25), 9 (2001).
5.
6.
7.
I. V. Ukrainets, E. A. Taran, O. I. Naboka, and I. V. Senyuk, Vestnik Farmatsii, No 4 (28), 16 (2001).
I. V. Ukrainets, E. A. Taran, L. N. Voronina, and O. I. Naboka, Farm. Zh., No. 6, 48 (2001).
E. Eriksoo, E. B. M. Sandberg, and L. J. T. Stalhandske, US Patent 4738971 (1988).
8.
K. Tsuji, G. W. Spears, K. Nakamura, T. Tojo, N. Seki, A. Sugiyama, and M. Matsuo, Bioorg. Med.
Chem. Lett., 12, 85 (2002).
9.
10.
S. R. Khan, A. Mhaka, R. Pili, and J. T. Isaacs, Bioorg. Med. Chem. Lett., 11, 451 (2001).
J. Shi, Z Xiao, M. A. Ihnat, C. Kamat, B. Pandit, Z. Hu. and P. Li, Bioorg. Med. Chem. Lett., 13, 1187
(2003).
11.
12.
13.
14.
15.
S. Jönsson. G. Andersson, T. Fex, T. Fristedt, G. Hedlund, K. Jansson, L. Abramo, I. Fritzson.
O. Pekarski, A. Runström, H. Sandin, I. Thuvesson, and A. Björk, J. Med. Chem., 47, 2075 (2004).
I. V. Ukrainets, S. G. Taran, O. V. Gorokhova, E. A. Taran, N. A. Jaradat, and I. Yu. Petukhova, Khim.
Geterotsikl. Soedin., 203 (2000). [Chem. Heterocycl. Comp., 36, 166 (2000)].
I. V. Ukrainets, S. G. Taran O. A. Evtifeeva, O. V. Gorokhova, N. I. Filimonova, and A. V. Turov,
Khim. Geterotsikl. Soedin., 204 (1995). [Chem. Heterocycl. Comp., 31, 176 (1995)].
W. Stadlbauer, R. Laschober, H. Lutschounig, G. Schindler, and T. Kappe, Monats. Chem., 123, 617
(1992).
I. V. Ukrainets, L. A. Petrushova, L. V. Sidorenko, V. B. Rybakov, and V. V. Chernyshev, Zh. Org.
Farm. Khim., 2, issue 3(7), 26 (2004).
16.
17.
18.
H.-B. Burgi and J. D. Dunitz, Struct. Correl., Vol. 4. VCH, Weinheim (1994), p. 741.
L. Collins and S. G. Franzblau, Antimicrob. Agents Chemother., 41, 1004 (1997).
S. H. Siddiqui in: H. D. Isenberg (editor), Clinical Microbiological Procedures Handbook, Vol. 1,
American Society for Microbiology, Washington D.C. (1992), p. 5.14.2.
19.
20.
21.
22.
L. B. Heifets in L. B. Heifets (editor), Chemistry of Mycobacterial Infections, CRC Press, Boca Raton
(1991), p. 89.
C. B. Inderleid and K. A. Nash in: V. Lorian (editor), Antibiotics in Laboratory Medicine, Williams and
Wilkins, Baltimore (1996), p. 127.
I. V. Ukrainets, O. V. Gorokhova, S. G. Taran, P. A. Bezuglyi, A. V. Turov, N. A. Marusenko, and
O. A. Evtifeeva, Khim. Geterotsikl. Soedin., 958 (1994). [Chem. Heterocycl. Comp., 30, 829 (1994)].
G. M. Sheldrick, SHELX97. PC Version. A System of Computer Programs for Crystal Structure Solution
and Refinement, Revision 2 (1998).
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