Collect. Czech. Chem. Commun.
2005, 70, 72-84
https://doi.org/10.1135/cccc20050072
Synthesis of β-D-Glucopyranosides of 6-Substituted 2-(Indol-3-yl)benzothiazoles
Martin Humeníka,*, Peter Kutschya, Katarína Valkováa, Branislav Horváthb, Vladimír Kováčikc and Slávka Bekešovác
a Institute of Chemical Sciences, Faculty of Science, P. J. Šafárik University, Moyzesova 11, 041 67 Košice, Slovak Republic
b Institute of Chemistry, Faculty of Science, Comenius University, Mlynská dolina CH-2, 842 15 Bratislava, Slovak Republic
c Institute of Chemistry, Slovak Academy of Sciences, Dúbravská cesta 9, 842 38 Bratislava, Slovak Republic
References
1. J. Chem. Soc. 1969, 2644.
B. J., Trask E. G.:
2a. J. Med. Chem. 1994, 37, 1689.
< M. F. G., McCall C. J., Lelieveld P., Alexander P., Richter A., Davies D. E.: https://doi.org/10.1021/jm00037a020>
2b. J. Med. Chem. 1996, 39, 3375.
< D. F., Bradshaw T. D., Wrigley S., McCall C. J., Lelieveld P., Fichtner I., Stevens M. F. G.: https://doi.org/10.1021/jm9600959>
2c. Br. J. Cancer 1998, 77, 745.
< T. D., Wrigley S., Shi D. F., Schultz R. J., Paull K. D., Stevens M. F. G.: https://doi.org/10.1038/bjc.1998.122>
2d. Curr. Med. Chem. 2001, 8, 203.
< T. D., Stevens M. F. G., Westwell A. D.: https://doi.org/10.2174/0929867013373714>
2e. J. Med. Chem. 1999, 42, 4172.
< E., Hutchinson I., Chua M. S., Stinson S. F., Phillips L. R., Kaur G., Sausville E. A., Bradshaw T. D., Westwell A. D., Stevens M. F. G.: https://doi.org/10.1021/jm990104o>
2f. J. Med. Chem. 2001, 44, 1446.
< I., Chua M. S., Browne H. L., Trapani V., Bradshaw T. D., Westwell A. D., Stevens M. F. G.: https://doi.org/10.1021/jm001104n>
2g. Tetrahedron Lett. 2000, 41, 425.
< I., Stevens M. F. G., Westwell A. D.: https://doi.org/10.1016/S0040-4039(99)02076-6>
2h. Br. J. Cancer 2002, 86, 1348.
< T. D., Chua M. S., Browne H. L., Trapani V., Sausville E. A., Stevens M. F. G.: https://doi.org/10.1038/sj.bjc.6600225>
2i. J. Med. Chem. 2002, 45, 744.
< I., Jennings S. A., Vishuvajjala B. R., Westwell A. D., Stevens M. F. G.: https://doi.org/10.1021/jm011025r>
3. Bioorg. Med. Chem. Lett. 2000, 41, 425.
B., Hong F., Kohm C., Bonham L., Klein P.:
4. Anti-Cancer Drugs 1997, 8, 489.
< J. Ch., Roffey R. A. J., Stephens A. M., StratPred J. I.: https://doi.org/10.1097/00001813-199706000-00012>
5a. Phytochemistry 2000, 53, 161.
< M. S. C., Okanga F. I., Zaharia I. L., Khan A. Q.: https://doi.org/10.1016/S0031-9422(99)00494-X>
5b. Tetrahedron 1991, 47, 3909.
< L. M., Conn K. L., Ayer W. A., Tewari J. P.: https://doi.org/10.1016/S0040-4020(01)86431-0>
5c. Plant Physiol. 1992, 98, 1304.
< J., Jackson E. P., Gaage D. A., Hammerschmidt R., Somervile S. C.: https://doi.org/10.1104/pp.98.4.1304>
6. Collect. Czech. Chem. Commun. 2004, 69, 1657.
< M., Dzurilla M., Kutschy P., Solčániová E., Kováčik V., Bekešová S.: https://doi.org/10.1135/cccc20041657>
7a. J. Med. Chem. 1971, 14, 248.
< J. P., Trigg R. B., Warrington J. V.: https://doi.org/10.1021/jm00285a022>
7b. Collect. Czech. Chem. Commun. 1999, 64, 1448.
< M., Ružinský M., Kutschy P., Tewari J. P., Kováčik V.: https://doi.org/10.1135/cccc19991448>
8a. Aust. J. Chem. 1955, 8, 545.
< K. J., Warburton W. K.: https://doi.org/10.1071/CH9550545>
8b. Synth. Commun. 1979, 9, 457.
< K. G., Jain S. K., Gupta R. R.: https://doi.org/10.1080/00397917908060947>
8c. Pharmazie 1991, 883.
P., Mathur V., Gupta V.:
8d. Pharmazie 1986, 830.
R. R., Kumar R.:
9. Collect. Czech. Chem. Commun. 2004, 69, 453.
< J., Dzurilla M., Kutschy P., Pazdera P., Kováčik V., Alföldi J., Bekešová S.: https://doi.org/10.1135/cccc20040453>
10a. Zh. Obshch. Khim. 1961, 2839.
N. N., Preobrazhenskaya M. N.:
10b. J. Org. Chem. 1968, 192.
< E., Holly F. W., Jenkins S. R.: https://doi.org/10.1021/jo01265a602>
10c. Tetrahedron 1972, 28, 3069.
< A. A., Stephen A. M.: https://doi.org/10.1016/0040-4020(72)80022-X>
10d. Zh. Obshch. Khim. 1965, 893.
M. N., Suvorov N. N.:
10e. Preobrazhenskaya M. N., Korbukh I. A. in: Chemistry of Nucleosides and Nucleotides (L. B. Townsend, Ed.); Vol. 3, p. 1. Plenum Press, New York 1994.
10f. Zh. Org. Khim. 1974, 10, 1764.
M. N., Tolkachev V. N., Geling O. N., Kostyuchenko P. P.:
11. Heterocycles 2001, 54, 425.
< M., Tanimoto A., Orita H., Yamada F., Ohta T.: https://doi.org/10.3987/COM-00-S(I)12>
12a. Org. Synth. 1984, 62, 158.
I. K., Scheibye S. C., Lawesson O. S.:
12b. Tetrahedron 1985, 41, 5061.
< P. M., Levinson I. M.: https://doi.org/10.1016/S0040-4020(01)96753-5>
13a. Ber. Dtsch. Chem. Ges. 1903, 36, 3121.
< A.: https://doi.org/10.1002/cber.19030360388>
13b. Sprague J. M., Land A. H. in: Heterocyclic Compounds (R. C. Elderfield, Ed.), Vol. 5, Chap. 8, p. 484. J. Wiley, New York 1957.
13c. Collect. Czech. Chem. Commun. 1994, 59, 2663.
< M., Kutschy P., Imrich J., Brtoš S.: https://doi.org/10.1135/cccc19942663>
13d. Collect. Czech. Chem. Commun. 1981, 46, 436.
< P., Dzurilla M., Kristián P., Kutschyová K.: https://doi.org/10.1135/cccc19810436>
14. J. Prakt. Chem. 1966, 31, 262.
< G.: https://doi.org/10.1002/prac.19660310503>
15. Bull. Chem. Soc. Jpn. 1970, 43, 2535.
< Y., Kurita K.: https://doi.org/10.1246/bcsj.43.2535>
16a. J. Org. Chem. 2001, 68, 22.
D. A., Luo C., Reitz B. A.:
16b. J. Org. Chem. 2003, 68, 8693.
< D. A., Luo C., Reitz B. A.: https://doi.org/10.1021/jo0349431>
17. J. Med. Chem. 1991, 34, 2588.
< R. S. J., Buckle R. D., Carey C., Parr-Dobrzanski H., Faller A., Foster A. K., Houge-Frydrych S. V. C., Pinto L. I., Smith G. D., Taylor S. G.: https://doi.org/10.1021/jm00112a037>
18a. Ber. Dtsch. Chem. Ges. 1886, 19, 1067.
< P.: https://doi.org/10.1002/cber.188601901239>
18b. Justus Liebigs Ann. Chem. 1929, 486, 188.
, Koch, Stuckenbrock:
18c. J. Org. Chem. 1966, 31, 1484.
< E. H., Woerther H.: https://doi.org/10.1021/jo01343a039>
18d. J. Med. Chem. 1991, 34, 1008.
B. L., Larson E. R., Beyer T. A., Zembowski W. J., Aldinger C. E.:
18e. Heterocycl. Commun. 2001, 7, 73.
< S. H., Kumar S., Nivalkar K. R.: https://doi.org/10.1515/HC.2001.7.1.73>