1. (a) Yildiz-Oren I., Yalcin I., Aki-Sener E., Ucarturk N. Eur. J. Med. Chem. 2004, 39, 291.
https://doi.org/10.1016/j.ejmech.2003.11.014
(b) Latrofa A., Franco M., Lopedota A., Rosato A., Carone D., Vitali C. II Farmaco 2005, 60, 291.
https://doi.org/10.1016/j.farmac.2005.01.010
2. Bell F.W., Cantrell A.S., Hoegberg M., Jaskunas S.R., Johansson N.G., Jordan C.L., Kinnick M.D., Lind P., Morin Jr. J.M. J. Med. Chem. 1995, 38, 4929.
https://doi.org/10.1021/jm00025a010
4. Goldfarb R.H., Kitson R.P., Brunson K.W., Yoshino K., Hirota N., Kirii Y., Inoue Y., Ohashi M. Anticancer Res. 1999, 19, 1663.
5. Amit B.N., Kamath R.V., Khadse G.B. Indian J. Heterocycl. Chem. 2000, 9, 309.
8. Miwatashi S., Arikawa Y., Kotani E., Miyamoto M., Naruo K.-I., Kimura H., Tanaka T., Asahi S., Ohkawa S. J. Med. Chem. 2005, 48, 5966.
https://doi.org/10.1021/jm050165o
13. Zhdanova K.A., Bragina N.A. Russ. Chem. Bull., Int. Ed. 2015, 64(10), 2294.
14. Herz R. U.S. Pat. 1, 1928, 699, 432, Chem. Abstr. 1929, 23, 1140.
16. Zubarovskii V.M. J. Gen. Chem. (USSR), 1947, 17, 613, Chem. Abstr. 1948, 42, 906.
17. Leaper J.M.F. J. Am. Chem. Soc. 1931, 53, 1891.
https://doi.org/10.1021/ja01356a040
(a) Cassella and Co., Ger. Pat., 367,344, Frdl., 1922, 14, 912. (b) Cassella and Co., Ger. Pat., 367,345, Frdl., 1922, 14, 914. (c) Cassella and Co., Ger. Pat., 367,346, Frdl., 1922, 14, 918. (d) Cassella and Co., Ger. Pat., 364,822, Frdl., 1922, 14, 920.
19. Cassella and Co., Ger. Pat., 360,690, Frdl., 1922, 14, 908.
22. Gupta V., Ph.D. Thesis, University of Rajasthan, Jaipur, India, 1990.
25. Weinberg H.V. Chim. Ztg. 1930, 42, 404.
30. Cauquil G., Cassadevall A. Bull. Soc. Chim. Fr. 1955, 768.
34. Bourdais J. French. Pat. 1966, 1,443,917, Chem. Abstr. 1967, 66, 37933.
39. Adams R. (Editor in chief) Organic Reactions. New York: John Wiley and Sons, 1959, 3, 240 and 1957, 3, 259.
52. (a) Kumar M., Sharma N., Gupta R., Gupta R.R. Heterocycl. Commun. 1998, 4(2), 187.
https://doi.org/10.1515/HC.1998.4.2.187
(b) Sharma P.K. Der Pharmacia Lettre 2016, 8(11), 140.
(c) Sharma P.K. Der Pharmacia Lettre 2016, 8(11), 79.
(d) Sharma P.K. Der Pharma Chemica 2016, 8(11), 156.
(e) Sharma P.K. Der Pharma Chemica 2016, 8(5), 191.
(f) Sharma P.K. Der Pharmacia Lettre 2016, 8(4), 86.
(g) Sharma P.K. Res. Chem. Intermed. 2015, 41(9), 6141.
https://doi.org/10.1007/s11164-014-1727-1
(h) Sharma P.K. Med. Chem. Res. 2012, 21(8), 2072.
https://doi.org/10.1007/s00044-011-9732-z
(i) Sharma P.K. Res. Chem. Intermed. 2011, 37(8), 1103.
https://doi.org/10.1007/s11164-011-0320-0
(j) Sharma P.K. Res. Chem. Intermed. 2010, 36(8), 985.
https://doi.org/10.1007/s11164-010-0211-9
(k) Sharma P.K. Synth. Commun. 2010, 40(16), 2347.
https://doi.org/10.1080/00397910903243807
(l) Sharma P.K. Res. Chem. Intermed. 2009, 35, 35.
https://doi.org/10.1007/s11164-008-0017-1
(m) Ankodia V., Sharma P.K., Sharma K., Kumar M., Gupta A. Hetrocycl. Commun. 2009, 15(2), 127.
https://doi.org/10.1515/HC.2009.15.2.127
(n) Sharma P.K. J. Chem. Pharm. Res. 2015, 7(11), 462.
(o) Sharma P.K. Drug Invent. Today 2017, 9(3), 18
–22.
(p) Sharma P.K. Drug Invent. Today 2017, 9(3), 23–25.
57. Bussiere D., Fang E., Murray J. (Chiron Corporation, USA). PCT Int. Appl. 2006, 228 p. WO 2006022718 A1 20060302.
58. Tomoji A., Kentarou K., PCT Int. Appl. 2008047694, 2008, 47 p.
59. Choudary B.M., Jeyalakshmi K., Aduri R., Kantam M.L. Indian Pat. Appl. 2003DE00405, 2007, 14 p.
60. Bessis A.S., Christelle B., Beatrice B., Mark E.J., Maria S. PCT Int. Appl. 2005123703, 2005, 308 p.
62. Chen J.L. PCT Int. Appl. 2005086904, 22 Sep 2005.
65. Chattopadhyay S., Shadakshari U., Talukdar S. Indian J. Chem. 2001, 40B(10), 1007.
66. Song Y.L., Chen Z.B. Jingxi Huagong, 2002, 19(1), 59–61.