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Green Chemistry
Page 6 of 6
ARTICLE
Green Chem., 2011, 13, 2365. (j) M. Araghi, V. Mirkhani, M.
Journal Name
1986, 672.
Moghadam, S. Tangestaninejad, I. Mohammdpoor-Baltork,
Dalton Trans., 2012, 41, 11745. (k) N. G. Khaligh, Rsc. Adv.,
2013, 3, 99. (l) Y.-Q. Zhangi, Y.-C. Li, J.-H. Zhu, Z.-F. Li, G.-Z.
Guo, D.-P. Chen, Asian J. Chem., 2014, 26, 7746. (m) Z. Liu, Q.
Ma, Y. Liu, Q. Wang, Org. Lett. 2014, 16, 236. (n) R. Qiu, G.
Zhang, Y. Zhu, X. Xu, L. Shao, Y. Li, D. An, S. Yin, Chem. Eur. J.,
2009, 15, 6488. (o) H. Sharghi, M. Jokar, M. M. Doroodmand,
Adv. Synth. Catal. 2011, 353, 426.
9
(a) B. C. Hamper, D. M. Snyderman, T.DJO. IO: 1w0e.1n0,39A/.DM0G.CS0c3a7t3e1sA,
D. C. Owsley, A. S. Kesselring, R. C. Chott, J. Comb. Chem. 1999,
1, 140. (b) P. Hermant, D. Bosc, C Piveteau, R. Gealageas, B.
Lam, C. Ronco, M. Roignant, H. Tolojanahary, L. Jean, P.-Y.
Renard, M. Lemdani, M. Bourotte, A. Herledan, C Bedart, A.
Biela, F. Leroux, B. Deprez, R. Deprez-Poulain, J. Med. Chem.,
2017, 60, 9067. (c) I. Im, E. S. Lee, S. J. Choi, J.-Y. Lee, Y.-C. Kim,
Bioorg. Med. Chem. Lett., 2009, 19, 3632.
3
(a) Q. M. Kainz, R. Linhardt, P. K. Maity, P. R. Hanson, O. Reiser,
Chem Sus Chem., 2013, 6, 721. (b) D. Chevella, N. Mamedaa, 10 (a) D. Prat, A. Wells, J. Hayler, H. Sneddon, C. R. McElroy, S.
S. Perak, S. Kodumuri, R. Banothu, N. Namaa, Catal. Commun.,
2016, 81, 29. (c) C. L. Allen, B. N. Atkinson, J. M. J. Williams,
Abou-Shehadad, P. J. Dunne, Green Chem., 2016, 18, 288. (b)
Denis Prat, J. Hayler, A. Wells, Green Chem., 2014, 16, 4546.
Angew. Chem. Int. Ed. 2012, 51, 1383. (d) R. Pelagalli, I. 11 (a) N. Blaquiere, D. G. Shore, S. Rousseaux, K. Fagnou, J. Org.
Chiarotto, M. Feroci, S. Vecchio, Green Chem., 2012, 14, 2251.
(e) S. N. Rao, D. C. Mohan, S. Adimurthy, Green Chem., 2014,
16, 4122. (f) A. Ojeda-Porras, A. Hernández-Santana, D.
Gamba-Sánchez, Green Chem., 2015, 17, 3157. (g) D. D. S.
Sharley, J. M. J. Williams, Chem. Commun., 2017, 53, 2020. (h)
A. H. Chowdhury, S. Ghosh, Sk. M. Islam, New J. Chem., 2018,
Chem. 2009, 74, 6190. (b) D. Z. Qiang, J. B. Shi, B. A. Songb, X.
H. Liu, Rsc Adv., 2014, 4, 5607. (c) S. P. Bew, G. R. Stephenson,
J. Rouden, J. Godemert, H. Seylani, L. A. Martinez-Lozano,
Chem. Eur. J. 2017, 23, 4557. (d) S. Singla, P. Piplani, Bioorg.
Med. Chem. Lett., 2016, 24, 4587. (e) Y. Ryu, A. I. Scott,
Tetrahedron Lett., 2003, 44, 7499.
42, 14194. (i) J. E. Taylor, M. D. Jones, J. M. J. Williams, S. D. 12 C. W. P. Lorencak J. Am. Chem. Soc. 1988, 110, 1880.
Bull, J. Org. Chem. 2012, 77, 2808. (j) M. Kumar, S. Sharma, K. 13 (a) B. Yo, B.-B. Cheng, W.-Q. Liu, W. Li, S.-S. Wang, J. Cao, C.-
Thakur, O. S. Nayal, V. Bhatt, M. S. Thakur, N. Kumar, B. Singh,
U. Sharma, Asian J. Org. Chem. 2017, 6, 342. (k) U. Mandi, A.
S. Roy, B. Banerjee, Sk. M. Islam, Rsc Adv., 2014, 4, 42670. (l)
M. Nardi, N. Herrera Cano, P. Costanzo, M. Oliverio, G.
Sindonaa, A. Procopioc, Rsc. Adv., 2015, 5, 18751. (m) H.
Morimoto, R. Fujiwara, Y. Shimizu, K. Morisaki, T. Ohshima,
Org. Lett. 2014, 16, 2018. (n) H. Sheng, R. Zeng, W. Wang, S.
Luo, Y. Feng, J. Liu, W. Chen, M. Zhu, Q. Guo, Adv. Synth.
Catal., 2017, 359, 302. (o) J.-F. Soul, H. Miyamura, S.
Kobayashi, Chem. Asian J. 2013, 8, 2614. (p) R. Murashige, Y.
Hayashi, S. Ohmori, A. Torii, Y. Aizu, Y. Muto, Y. Murai, Y. Oda,
M. Hashimoto, Tetrahedron, 2011, 67, 641.(q) B. R. Kim, G. H.
Sung, S.-G. Lee, Y. J. Yoon, Tetrahedron, 2013, 69, 3234. (r) J.
E. Taylor, J. M. J. Williams, S. D. Bull, Tetrahedron Lett., 2012,
53, 4074. (s) T. Kitayama, S. Isomori, K. Nakamura,
Tetrahedron Asymmetry, 2013, 24, 621. (t) M. Kumar, S.
Bagchi, A. Sharma, New J. Chem., 2015, 39, 8329. (u) Y.-C.
Yang, D. Y. C, Leung, P. H. Toy, Synlett, 2013, 24, 1870. (v) S.
Magens, M. Ertelt, A. Jatsch, B. Plietker, Org. Lett., 2008, 10,
53. (w) X.-Y. Zhou, X. Chen, Synlett, 2018, 29, 2321. (x) B.
Sarmah, R. Srivastava, ACS Sustainable Chem. Eng. 2015, 3,
210. (y) b. R. Kilm,,,Gi. H. Sung, K. E. Ryu, H. J. Yoon, S.-G. Lee,
Y.-J. Yoon, Synlett, 2014, 25, 1909.
(a) R. H. Baker, F. G. Bordewell, Org. Synth. Coll., Vol. 3; ed. E.
C. Horning, John Wiley and Sons, New York, 1955, 141; (b) K.
Ishihara, M. Kubota, H. Kurihara, H.Yamamoto, J. Org. Chem.,
1996, 61, 4560. (c) A. Orita, C. Tanahashi, A. Kakuda, J. Otera,
Angew. Chem., Int. Ed., 2000, 39, 2877. (d) R. Varala, A.
Nasreen, S. R. Adapa, Can. J. Chem., 2007, 85, 148.
for selected recent reports see: (a) J. Zhang, Q. Qian, Y. Wang,
B. B. A. Bediako, M. Cui, G. Yanga, Buxing Han, Green Chem.,
2019, 21, 233. (b) P. Sreenivasulu, C. Pendemb, N.
Viswanadham, Nanoscale, 2014, 6, 14898. (c) S. Bongarzone,
A. Runser, C. Taddei, A. K. Haji Dheere, A. D. Gee, Chem.
Commun., 2017, 53, 5334.
W Hu, Adv. Synth. Catal. 2016, 358, 90. (b) B.-B. Cheng, B. Yu,
C.-W. Hu, Rsc Adv., 2016, 6, 87179. (c) T. Yang, H. Lu, R. Qiu, L.
Hong, S.F. Yin, N. Kambe, Chem.Asian J., 2019, 14, 1436. (d) N.
Mase, T. Horibe, Org. Lett., 2013, 15, 1854.
4
5
6
7
(a) A. N. Meldrum, J. Chem. Soc.1, 908, 93, 598. (b) A. R. Butler,
J. Chem. Res. ( S ) , 1978, 50, 855.
(a) J.-S. Li, Y.-D. Da, G.-Q. Chen, Q. Yang, Z.-W. Li, F. Yang, P.-
M. Huang, Chemistry Select 2017, 2, 1770. (b) I. Mierina, A.
Stikute, A. Mishnev, M. Jure Monatshefte für Chemie, 2019,
150, 85. (c) J. Li, Y. Da, G. Chen, C. Liu, W. Zhang, 2019, CN
106278924 A 20170104.
For the synthesis of formyl acetic esters from alcohol and
formyl Meldrum’s acid, see: (a) L. Buschbeck and J.
Christoffers J. Org. Chem., 2018, 83, 4002. (b) N. D. Obushak,
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