B(C6F5)3-catalyzed synthesis of coumarins via Pechmann condensation under solvent-free…
473
28. Shirini F, Marjani K, Nahzomi HT (2007) Chin Chem Lett 18:909
29. Rezaei R, Dorosty L, Rajabzadeh M, Khalifeh R (2011) Chin
Chem Lett 22:1313
temperature, was poured onto 40 g crushed ice and stirred
for 5–10 min. The solid products were fltered of, washed
with ice-cold water, and recrystallized from hot ethanol to
aford pure coumarin derivatives 3. The known compounds
were identifed by comparison of their spectral data and
physical properties with the reported literature.
30. Karami B, Kiani M (2011) Catal Commun 14:62
31. Nazeruddin GM, Pandharpatte MS, Mulani KB (2012) C R Chim
15:91
32. Albadi J, Shirini F, Abasi J, Armand N, Motaharizadeh T (2013)
C R Chim 16:407
33. Li S, Qi X, Huang B (2016) Catal Today 276:139
34. Li TS, Zhang ZH, Yang F, Fu CG (1998) J Chem Res (S) 38
35. Abbasi Z, Rezayati S, Bagheri M, Hajinasiri R (2017) Chin Chem
Lett 28:75
Acknowledgements The authors thank to NIPER, Hyderabad & Ino-
vine Pharma Research Solution, Raipur for the scientifc and instru-
mental support.
36. Sharma RK, Monga Y, Puri A (2013) Catal Commun 35:110
37. Zareyee D, Serehneh M (2014) J Mol Catal A: Chem 391:88
38. Yadav GD, Ajgaonkar NP, Varma A (2012) J Catal 292:99
39. Ahmed AI, El-Hakam SA, Khder AS, Abo El-Yazeed WS (2013)
J Mol Catal A: Chem 366:99
References
1. Murray R (1995) Nat Prod Rep 12:477
40. Reddy BM, Patil MK, Lakshmanan P (2006) J Mol Catal A: Chem
256:290
2. Scheel LD (1972) Microbiol Toxins 8:47
3. Sun WC, Gee KR, Haugland RP (1998) Bioorg Med Chem Lett
8:3107
41. Naik MA, Mishra BG, Dubey A (2008) Colloids Surf A 317:234
42. Ghodke S, Chudasama U (2013) Appl Catal A 453:219
43. Jadhav NH, Sakate SS, Rasal NK, Shinde DR, Pawar RA (2019)
ACS Omega 4:8522
4. Wang CJ, Hsieh YJ, Chu CY, Lin YL, Tseng TH (2002) Cancer
Lett 183:163
5. Bravic G, Gaultier J, Hauw C (1968) C R Acad Sci. Paris Ser IIc:
Chim 267:1790
44. Potdar MK, Mohile SS, Salunkhe MM (2001) Tetrahedron Lett
42:9285
6. Arora RB, Mathur CN (1963) Br J Pharmacol Chemother 20:29
7. Palmer CJ, Josephs JL (1995) J Chem Soc Perkin Trans 1:3135
8. Maddi V, Kallur RS, Rao MNA (1992) J Pharm Sci 81:964
9. Musiciki B, Periers AM, Laurin P, Ferroud D, Benedetti Y,
Lachaud S, Chatreaux F Haesslein JL, LLtis A, Pierre C, Khider
J, Tessol N, Airault M Demassey J, Dupuis-Hamelin C Lassaigne
P, Bonnefoy A, Vicat P, Klich M (2000) Bioorg Med Chem Lett
10:1695
45. Frere S, Thiery V, Besson T (2001) Tetrahedron Lett 42:2791
46. Romanelli GP, Bennardi D, Ruiz DM, Baronetti G, Thomas HJ,
Autino JC (2004) Tetrahedron Lett 45:8935
47. Laufer MC, Hausmann H, Holderich WF (2003) J Catal 218:315
48. Khaligh NG (2012) Catal Sci Technol 2:1633
49. Maheswara M, Siddaiah V, Damu GLV, Rao YK, Rao CV (2006)
J Mol Catal A: Chem 255:49
50. Russell A, Frye JR (1941) Org Synth 21:22
51. Simmonis H, Remmert P (1914) Chem Ber 47:2229
52. Chandrasekhar S, Reddy CR, Chandrashekar G (2004) Tetrahe-
dron Lett 45:6481
10. Pechmann HV, Duisberg C (1884) Ber Dtsch Chem Ges 17:929
11. Johnson JR (1942) Org React 1:210
12. Shirner RL (1942) Org React 1:1
13. Brufola G, Fringuelli F, Piermatti O, Pizzo F (1996) Heterocycles
43:1257
53. Chandrasekhar S, Reddy CR, Babu BN, Chandrashekar G (2002)
Tetrahedron Lett 43:3801
14. Yavari I, Hekmat-Shoar, Zonouzi A (1998) Tetrahedron Lett
39:2391
54. Thirupathi P, Neupane LN, Lee KH (2011) Tetrahedron 67:7301
55. Chandrasekhar S, Chandrashekar G, Vijeender K, Reddy MS
(2006) Tetrahedron Lett 47:3475
15. Molnar M, Lončarić M, Kovač M (2020) Curr Org Chem 24:4
16. Appel H (1935) J Chem Soc 1031
56. Chandrasekhar S, Reddy CR, Babu BN (2002) J Org Chem
67:9080
17. Woods LL, Sapp J (1962) J Org Chem 27:3703
18. Ahmad ZS, Desai RD (1937) Proc Indian Acad Sci Chem Sci
5:277
57. Prajapti SK, Nagarsenkar A, Babu BN (2014) Tetrahedron Lett
55:3507
19. Robinson R, Weygand F (1941) J Chem Soc 386
20. Nadkarni AJ, Kudav NA (1981) Ind J Chem Sect B 20:719
21. Valizadeha H, Shockravi A (2005) Tetrahedron Lett 46:3501
22. Bahekar SS, Shinde DB (2004) Tetrahedron Lett 45:7999
23. Karami B, Kiani M, Hoseini MA (2014) Chin J Catal 35:1206
24. Peng MM, Hemalatha P, Ganesh M, Palanichamy M, Jang HT
(2014) J Ind Eng Chem 20:953
58. Prajapti SK, Nagarsenkar A, Babu BN (2014) Tetrahedron Lett
55:1784
59. Guggilapu SD, Prajapti SK, Babu BN (2015) Tetrahedron Lett
56:889
60. Nagarsenkar A, Prajapti SK, Babu BN (2015) J Chem Sci 127:711
61. Prajapti SK, Gupta KK, Babu BN (2015) J Chem Sci 127:1047
25. Sudha S, Venkatachalam K, Vishnu Priya S, Herbert Mabel J,
Palanichamy M, Murugesan V (2008) J Mol Catal A: Chem
291:22
Publisher’s Note Springer Nature remains neutral with regard to
jurisdictional claims in published maps and institutional afliations.
26. Heravi MM, Khorasani M, Derikvand F, Oskooie HA, Bamohar-
ram FF (2007) Catal Commun 8:1886
27. Torviso R, Mansilla D, Belizan A, Alesso E, Moltrasio G,
Vazquez P, Pizzio L, Blanco M, Caceres C (2008) Appl Catal A
339:53
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