RSC Advances
Paper
AIIMS, New Delhi, India for TEM analysis. SKA is also thankful 27 Z. Chen, R. Fu, W. Chai, H. Zheng, L. Sun, Q. Lu and R. Yuan,
to the SERB (F/9974/20-17) and University of Delhi for generous
Tetrahedron, 2014, 70, 2237–2245.
nancial support.
28 M. Nirmala, G. Prakash, P. Viswanathamurthi and
J. G. Malecki, J. Mol. Catal. A: Chem., 2015, 403, 15–26.
29 B. Karami, M. Farahi and F. Pam, Tetrahedron Lett., 2014, 55,
6292–6296.
References
1 X. F. Li, X. G. Zhang, F. Chen and X. H. Zhang, J. Org. Chem.,
2018, 83, 12815–12821.
30 S. K. Rasheed, D. N. Rao, A. S. Reddy, R. Shankar and P. Das,
RSC Adv., 2015, 5, 10567–10574.
2 I. M. Dowine, M. J. Earle, H. Heaney and K. F. Shuhaibar,
Tetrahedron, 1993, 49, 4015–4034.
31 S. P. Pathare, R. V. Sawant and K. G. Akamanchi, Tetrahedron
Lett., 2012, 53, 3259–3263.
3 K. P. Dhake, P. J. Tambade, R. S. Singhal and B. M. Bhanage,
Green Chem. Lett. Rev., 2011, 4, 151–157.
4 S. L. Yedage, D. S. Dsilva and B. M. Bhanage, RSC Adv., 2015,
5, 80441–80449.
32 M. Rahman, D. Kundu, A. Hajra and A. Majee, Tetrahedron
Lett., 2010, 51, 2896–2899.
33 S. Joseph, P. Das, B. Srivastava, H. Nizar and M. Prasad,
Tetrahedron Lett., 2013, 54, 929–931.
5 R. B. Sonawane, N. K. Rasal and S. V. Jagtap, Org. Lett., 2017,
19, 2078–2081.
34 P. Singh, P. Yadav, A. Mishra and S. K. Awasthi, ACS Omega,
2020, 5, 4223–4232.
6 S. Kobayashi and K. Nishio, J. Org. Chem., 1994, 59, 6620–
6628.
35 S. Fortun and A. R. Schmitzer, ACS Omega, 2018, 3, 1889–
1896.
7 K. Shu, Y. Masaru and H. Iwao, Chem. Lett., 1996, 25, 407–
408.
36 M. Beygzadeh, A. Alizadeh, M. M. Khodaei and
D. Kordestani, Catal. Commun., 2013, 32, 86–91.
37 K. Nakajima and M. Hara, ACS Catal., 2012, 2, 1296–1304.
38 N. Koukabi, E. Kolvari, M. A. Zolgol, A. Khazaei, B. S
Shaghasemi and B. Fasahati, Adv. Synth. Catal., 2012, 354,
2001–2008.
39 A. Rahmatpour, Catal. Lett., 2012, 142, 1505–1511.
40 Hazards in the chemical laboratory, ed. S. G. Luxon, Royal
Society of Chemistry, Cambridge, 1992, p. 302.
41 H. Singh, J. K. Rajput and P. Arora, RSC Adv., 2016, 6, 84658–
84671.
42 Z. Wang, j. Xie, M. Shen, S. Nie and M. Xie, Trends Food Sci.
Technol., 2018, 74, 147–157.
43 Z. G. Wang and M. Lu, RSC Adv., 2014, 4, 1234–1240.
44 C. Garkoti, J. Shabir and S. Mozumdar, New J. Chem., 2017,
41, 9291–9298.
8 B.
Das,
M.
Krishnaiah,
P.
Balasubramanyam,
B. Veeranjaneyulu and D. N. Kumar, Tetrahedron Lett.,
2008, 49, 2225–2227.
9 P. Ju, J. Chen, A. Chen, L. Chen and Y. Yu, ACS Sustainable
Chem. Eng., 2017, 5, 2516–2528.
10 M. Waki and J. Meinhofer, J. Org. Chem., 1977, 42, 2019–
2020.
11 F. M. F. Chen and L. N. Benoiton, Synthesis, 1979, 9, 709–710.
12 S. H. Jung, J. H. Ahn, S. K. Park and J. K. Choi, Bull. Korean
Chem. Soc., 2002, 23, 149–150.
13 R. B. Sonawane, N. K. Rasal and S. V. Jagtap, Org. Lett., 2017,
19, 2078–2081.
14 P. Strazzolini, A. G. Giumanini and S. Cauci, Tetrahedron,
1990, 46, 1081–1118.
15 P. G. Reddy, G. D. K. Kumar and S. Baskaran, Tetrahedron
Lett., 2000, 41, 9149–9151.
45 M. Z. Kassaee, H. Masrouri and F. Movahedi, Appl. Catal., A,
2011, 395, 28–33.
16 F. F. Blicke and C. J. Lu, J. Am. Chem. Soc., 1952, 74, 3933–
3934.
46 D. Azarifar, O. Badalkhani and Y. Abbasi, J. Sulfur Chem.,
2016, 37, 656–673.
17 J. Deutsch, R. Eckelt, A. Kockritz and A. Martin, Tetrahedron,
2009, 65, 10365–10369.
47 N. Azizi, M. Edrisi and F. Abbasi, Appl. Organomet. Chem.,
2018, 32, 3901.
18 N. Shah, E. Gravel, D. V. Jawale, E. Doris and
I. N. N. Namboothiri, ChemCatChem, 2014, 6, 2201–2205.
19 L. B. Figueroa, A. O. Porras and D. G. Sanchez, J. Org. Chem.,
2014, 79, 4544–4552.
20 D. W. Gu and X. X. Guo, Tetrahedron, 2015, 71, 9117–9122.
21 A. C. shekhar, A. R. kumar, G. Sathaiah, V. L. paul,
M. Sridhar and P. S. rao, Tetrahedron Lett., 2009, 50, 7099–
7101.
48 F. Pakpour-Roudsari, M. Seddighi, F. Shirini and H. Tajik,
ChemistrySelect, 2019, 4, 6382–6389.
49 M. Tajbakhsh, H. Alinezhad, M. Nasrollahzadeh and
T. A. Kamali, J. Colloid Interface Sci., 2016, 471, 37–47.
50 V. K. Das, R. R. Devi, P. K. Raul and A. J. Thakur, Green
Chem., 2012, 14, 847–854.
51 A. P. Marjani, S. A. Hosseini, Z. Shokri and N. Maleki, Res.
Chem. Intermed., 2017, 43, 413–422.
22 M. H. Sarvari and H. Sharghi, J. Org. Chem., 2006, 71, 6652–
6654.
52 D. Habibi, S. Heydari and M. Afsharfarnia, Appl. Organomet.
Chem., 2017, 31, 3874.
23 N. Shah, E. Gravel, D. V. Jawale, E. Doris and
I. N. N. Namboothiri, ChemCatChem, 2014, 6, 2201–2205.
24 J. G. Kim and D. O. Jang, Synlett, 2010, 8, 1231–1234.
25 S. M. Sajadi, M. Maham and A. Rezaei, Lett. Org. Chem., 2014,
11, 49–54.
53 M. Kooti and E. Nasiri, J. Mol. Catal. A: Chem., 2015, 406,
168–177.
54 L. Ma’mani, M. Sheykhan, A. Heydari, M. Faraji and
Y. Yamini, Appl. Catal., A, 2010, 377, 64–69.
26 Y. J. Kim, J. W. Lee, H. J. Lee, S. Zhang, J. S. Lee, M. Cheong
and H. S. Kim, Appl. Catal., A, 2015, 506, 126–133.
41236 | RSC Adv., 2020, 10, 41229–41236
This journal is © The Royal Society of Chemistry 2020