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Chemical Science
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Acknowledgements
13724.
30 S. Mondal, S. R. Yetra, S. Mukherjee anDdOAI:.1T0..1B0i3ju9,/DA1cScC.0C2h8e19mG.
Res., 2019, 52, 425–436.
31 S. Mondal, S. R. Yetra, A. T. Biju, N-Heterocyclic Carbene-
Catalyzed Stetter Reaction and Related Chemistry. In N-
Heterocyclic Carbenes in Organocatalysis; Biju, A. T., Eds.;
Wiley-VCH: 2019; pp 59−93, ISBN: 9783527809042.
32 Y. B. Wang, Y. M. Wang, W. Z. Zhang, X.B. Lu, J. Am. Chem. Soc.
2013, 135, 11996−12003.
SKM thanks the STARS Program (Grant No. MoE-STARS/STARS-
1/473) of India. SM thanks CSIR, Delhi (09/921(0233)/2019-
EMR-I) for a research fellowship. AD thanks IISER Kolkata for a
research fellowship. SM thanks Jasimuddin Ahmed, IISER-
Kolkata, for his help in theoretical calculation. The authors also
thank Prof. T. K. Paine, IACS Kolkata, for X-ray facility.
33 V. B. Saptal, B. M. Bhanage, ChemSusChem, 2016, 9,
1980−1985.
34 S. Naumann, A. W. Thomas, A. P. Dove, Angew. Chem., Int. Ed.
2015, 54, 9550−9554.
35 U. Kaya, U. P. N. Tran, D. Enders, J. Ho, T.V. Nguyen, Org. Lett.
2017, 19, 1398−1401.
36 M. M. Hansmann, P.W. Antoni, H. Pesch, Angew. Chem., Int.
Ed. 2020, 59, 5782−5787.
37 P. W. Antoni, C. Golz, J. J. Holstein, D. A. Pantazis, M. M.
Hansmann, Nat. Chem. 2021, DOI: 10.1038/s41557-021-
00675-5.
38 S. G. Davies, A. M. Fletcher, P. M. Roberts, J. E. Thomson, Eur.
J. Org. Chem. 2019, 5093–5119.
39 P. Kothandaraman, S. J. Foo and P. W. H. Chan, J. Org. Chem.,
2009, 74, 5947-5952.
40 L. Qiuming H. Kasumi S. Datong, Organometallics 2020, 39,
22, 4115–4122.
41 S. C. Sau, R. Bhattacharjee, P.K. Hota, P. K. Vardhanapu, G.
Vijaykumar, R. Govindarajan, A. Datta, S.K. Mandal, Chem. Sci.
2019, 10, 1879−1884.
42 P. Eisenberger, B.P. Bestvater, E.C Keske, C. Crudden, Angew.
Chem., Int. Ed. 2015, 54, 2467−2471.
43 C. Chauvier, A. Tlili, C.Das Neves Gomes, P. Thuéry, T. Cantat,
Chem. Sci. 2015, 6, 2938−2942.
44 A. G. M. Barrett, M. R. Crimmin, M. S. Hill, P. B. Hitchcock and
P. A. Procopiou, Organometallics, 2007, 26, 4076-4079.
45 D. J. Liptrot, M. S. Hill, M. F. Mahon and A. S. S. Wilson, Angew.
Chem., Int. Ed., 2015, 54, 13362–13365.
Note and references
1
2
3
T. Sakakura, J.-C. Choi, H. Yasuda, Chem. Rev. 2007, 107,
2365−2387.
M. Aresta, A. Dibenedetto, A. Angelini, Chem. Rev. 2014, 114,
1709− 1742.
Y. Li, X. Cui, K. Dong, K. Junge, M. Beller, ACS Catal. 2017, 7,
1077− 1086.
4
5
P. Sreejyothi, S. K. Mandal, Chem. Sci. 2020, 11, 10571−10593.
C. D. N. Gomes, O. Jacquet, C. Villiers, P. Thuery, M.
Ephritikhine, T. Cantat, Angew. Chem., Int. Ed. 2012, 51,
187−190.
R. A. Pramudita, K. Motokura, Green Chem. 2018, 20,
4834−4843.
6
7
8
S. Bontemps, Coord. Chem. Rev. 2016, 308, 117−130.
E. J. Barreiro, A.E. Kümmerle, A. C. Fraga, Chem. Rev. 2011,
111, 5215−5246.
M. F. Ali, M. F. Ali and J. G. Speight, Handbook of Industrial
Chemistry: Organic Chemicals, McGraw-Hill Education, 2005.
9
10 T. H. Clarke, B. H. Gillespie, S. Z. Weisshaus, J. Am. Chem. Soc.
1933, 55, 4571−4587.
11 P. Tundo, M. Selva, Acc. Chem. Res. 2002, 35, 706−716.
12 O. Jacquet, X. Frogneux, C. D. N. Gomes, T. Cantat, Chem. Sci.
2013, 4, 2127−2131.
13 Y. Li, X. Fang, K. Junge, M. Beller, Angew. Chem. Int. Ed. 2013,
52, 9568−9571.
14 M.-Y. Wang, N. Wang, X.-F. Liu, C. Qiao, L.-N. He, Green Chem.
2018, 20, 1564−1570.
15 R. H. Lam, C. M. A. McQueen, I. Pernik, R. T. McBurney, A. F.
Hill, B. A. Messerle, Green Chem. 2019, 21, 538−549.
16 L.-G. Sebastian, M. Flores-Alamo, J. J. García, Organometallics
2015, 34, 763−769.
46 A. Das, J. Ahmed, N. M. Rajendran, D. Adhikari, S. K. Mandal,
J. Org. Chem. 2021, 86, 1, 1246–1252.
17 C. Lu, Z. QiU, Y. Zhu, B. L- Lin, Science Bulletin, 2019, 64, 11,
723-729.
18 X.F. Liu, C. Qiao, X.-Y. Li, L.-N. He, Green Chem. 2017, 19,
1726− 1731.
19 Z. Huang, X. Jiang, S. Zhou, P. Yang, C.-X. Du, Y. Li,
ChemSusChem, 2019, 12, 3054−3059.
20 W.-D. Li, D.-Y. Zhu, G. Li, J. Chen, J.-B. Xia, Adv. Synth. Catal.
2019, 361, 5098−5104.
21 C. Fang, C. Lu, M. Liu, Y. Zhu, Y. Fu, B.-L. Lin, ACS Catal. 2016,
6, 7876−7881.
22 F. Bobbink, S. Das, P. Dyson, Nat Protoc. 2017, 12, 417–428.
23 Z. Yang, B. Yu, H. Zhang, Y. Zhao, G. Ji, Z. Ma, X. Gao, Z. Liu,
Green Chem. 2015, 17, 4189−4193.
24 X.-F. Liu, X.Y. Li, C. Qiao, H.-C. Fu, L.-N. He, Angew. Chem., Int.
Ed. 2017, 56, 7425−7429.
25 X-F. Liu, X-Y. Li, C. Qiao, L-N. He, Synlett 2018, 29 (05), 548-
555.
26 E. Blondiaux, J. Pouessel, T. Cantat, T Angew. Chem., Int. Ed.
2014, 53, 12186−12190.
27 W.-C. Chen, J.-S. Shen, T. Jurca, C.-J. Peng, Y.-H. Lin, Y.-P.
Wang, W.-C. Shih, G.P.A. Yap, T.-G. Ong, Angew. Chem., Int.
Ed. 2015, 54, 15207−15212.
28 N. Kuhn, H. Bohnen, J. Kreutzberg, D. Blaser, R. Boese, J.
Chem. Soc., Chem. Commun. 1993, 1136 −1137.
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