Catalysis Science & Technology
Paper
2
(a) A. McKillop, D. Koyunçu, A. Krief, W. Dumont, P. Renier
and M. Trabelsi, Tetrahedron Lett., 1990, 31, 5007; (b) M.
Bagheri, N. Azizi and M. R. Saidi, Can. J. Chem., 2005, 83,
Tomar, M. R. Detty and S. Kumar, Org. Biomol. Chem.,
2014, 12, 1215; ( f ) A. J. Pacuła, F. Mangiavacchi, L.
Sancineto, E. J. Lenardão, J. Ścianowski and C. Santi, Curr.
Chem. Biol., 2015, 9, 97; (g) S. Kumar, J. Yan, J. Poon, V. P.
Singh, X. Lu, M. Karlsson Ott, L. Engman and S. Kumar,
Angew. Chem., Int. Ed., 2016, 55, 3729; (h) E. J. Lenardão, C.
Santi and L. Sancineto, in New Frontiers in Organoselenium
Compounds, ed. E. J. Lenardão, C. Santi and L. Sancineto,
Springer International Publishing, Cham, 2018, pp. 99–143;
(i) R. Kadu, M. Batabyal, H. Kadyan, A. L. Koner and S.
Kumar, Dalton Trans., 2019, 48, 7249–7260.
1
46.
3
4
5
(a) A. R. Ramesha and S. Chandrasekaran, J. Org. Chem.,
1
1
994, 59, 1354; (b) N. Iranpoor and B. Zeynizadeh, Synthesis,
999, 49.
(a) C. N. Yiannios and J. V. Karabinos, J. Org. Chem.,
963, 28, 3246; (b) R. Sanz, R. Aguado, M. R. Pedrosa and
1
F. J. Arnáiz, Synthesis, 2002, 856.
(a) S. M. S. Chauhan, A. Kumar and K. A. Srinivas, Chem.
Commun., 2003, 2348; (b) A. Dhakshinamoorthy, M. Alvaro
and H. Garcia, Chem. Commun., 2010, 46, 6476; (c) A. Corma,
T. Ródenas and M. J. Sabater, Chem. Sci., 2012, 3, 398; (d) A.
Dhakshinamoorthy, S. Navalon, D. Sempere, M. Alvaro and
H. Garcia, ChemCatChem, 2013, 5, 241; (e) C. Bottecchia, N.
Erdmann, P. M. A. Tijssen, L.-G. Milroy, L. Brunsveld, V.
Hessel and T. Noël, ChemSusChem, 2016, 9, 1781; ( f ) Y.
Dou, X. Huang, H. Wang, L. Yang, H. Li, B. Yuan and G.
Yang, Green Chem., 2017, 19, 2491; (g) H. Huang, J. Ash and
J. Y. Kang, Org. Biomol. Chem., 2018, 16, 4236.
10 (a) K. Arai, K. Dedachi and M. Iwaoka, Chem. – Eur. J.,
2011, 17, 481; (b) K. Arai, K. Moriai, A. Ogawa and M.
Iwaoka, Chem. – Asian J., 2014, 9, 3464; (c) K. Arai, H. Ueno,
Y. Asano, G. Chakrabarty, S. Shimodaira, G. Mugesh and M.
Iwaoka, ChemBioChem, 2018, 19, 207.
11 V. Rathore, A. Upadhyay and S. Kumar, Org. Lett., 2018, 20,
6274.
12 K. Arai, F. Kumakura, M. Takahira, N. Sekiyama, N. Kuroda,
T. Suzuki and M. Iwaoka, J. Org. Chem., 2015, 80, 5633.
13 K. Arai, A. Tashiro, Y. Osaka and M. Iwaoka, Molecules,
2017, 22, 354.
6
(a) J. L. G. Ruano, A. Parra and J. Alemán, Green Chem.,
2
008, 10, 706; (b) D. Singh, F. Z. Galetto, L. C. Soares,
O. E. D. Rodrigues and A. L. Braga, Eur. J. Org. Chem.,
010, 2010, 2661; (c) M. Oba, K. Tanaka, K. Nishiyama and
14 (a) A. Müller, E. Cadenas, P. Graf and H. Sies, Biochem.
Pharmacol., 1984, 33, 3235; (b) A. Wendel, M. Fausel, H.
Safayhi, G. Tiegs and R. Otter, Biochem. Pharmacol.,
1984, 33, 3241.
15 F. Kumakura, B. Mishra, K. I. Priyadarsini and M. Iwaoka,
Eur. J. Org. Chem., 2010, 2010, 440.
2
W. Ando, J. Org. Chem., 2011, 76, 4173; (d) E. Rattanangkool,
W. Krailat, T. Vilaivan, P. Phuwapraisirisan, M.
Sukwattanasinitt and S. Wacharasindhu, Eur. J. Org. Chem.,
2
014, 2014, 4795; (e) A. Talla, B. Driessen, N. J. W. Straathof,
16 (a) C. W. Nogueira, G. Zeni and J. B. T. Rocha, Chem. Rev.,
2004, 104, 6255; (b) E. E. Alberto, V. do Nascimento and
A. L. Braga, J. Braz. Chem. Soc., 2010, 21, 2032; (c) D. Tanini,
A. Grechi, L. Ricci, S. Dei, E. Teodori and A. Capperucci, New
J. Chem., 2018, 42, 6077.
17 E. L. Borges, M. T. Ignasiak, Y. Velichenko, G. Perin, C. A.
Hutton, M. J. Davies and C. H. Schiesser, Chem. Commun.,
2018, 54, 2990.
L.-G. Milroy, L. Brunsveld, V. Hessel and T. Noël, Adv. Synth.
Catal., 2015, 357, 2180; ( f ) S. S. Shah, S. Karthik and
N. D. P. Singh, RSC Adv., 2015, 5, 45416; (g) L. Bettanin, S.
Saba, F. Z. Galetto, G. A. Mike, J. Rafique and A. L. Braga,
Tetrahedron Lett., 2017, 58, 4713; (h) L. V. Lutkus, H. E.
Irving, K. S. Davies, J. E. Hill, J. E. Lohman, M. W. Eskew,
M. R. Detty and T. M. McCormick, Organometallics, 2017, 36,
2
588.
18 M. D. Milton, S. Khan, J. D. Singh, V. Mishra and B. L.
Khandelwal, Tetrahedron Lett., 2005, 46, 755.
19 Y. You, K. Ahsan and M. R. Detty, J. Am. Chem. Soc.,
2003, 125, 4918.
7
8
S. Salvador and R. J. Y. Chang, in Folding of Disulfide
Proteins, ed. R. J. Y. Chang and S. Ventura, Springer-Verlag,
New York, 2011, ch. 1, pp. 1–22.
(a) P. Krishnamurthy and A. Wadhwani, in Antioxidant
Enzymes, ed. M. A. El-Missiry, IntechOpen, London, 2012,
ch. 1, pp. 3–18; (b) B. Poljsak and I. Mili, in Oxidative Stress
and Chronic Degenerative Diseases - A Role for Antioxidants,
ed. J. A. Morales-González, IntechOpen, London, 2013, ch.
20 S. R. Wilson, P. A. Zucker, R. R. C. Huang and A. Spector,
J. Am. Chem. Soc., 1989, 111, 5936.
21 V. Nascimento, E. E. Alberto, D. W. Tondo, D. Dambrowski,
M. R. Detty, F. Nome and A. L. Braga, J. Am. Chem. Soc.,
2011, 134, 138.
1
4, pp. 331–353.
22 (a) B. Ahmed, D. Barrow and T. Wirth, Adv. Synth. Catal.,
2006, 348, 1043; (b) B. Ahmed-Omer, D. Barrow and T.
Wirth, Chem. Eng. J., 2008, 135, S280; (c) B. Ahmed-Omer,
D. A. Barrow and T. Wirth, Tetrahedron Lett., 2009, 50, 3352;
(d) X. Tang, R. K. Allemann and T. Wirth, Eur. J. Org. Chem.,
2017, 2017, 414; (e) K. Wang, L. Li, P. Xie and G. Luo, React.
Chem. Eng., 2017, 2, 611.
9
(a) W. J. Lees, Curr. Opin. Chem. Biol., 2008, 12, 740; (b)
K. P. Bhabak and G. Mugesh, Acc. Chem. Res., 2010, 43,
1
408; (c) X. Huang, X. Liu, Q. Luo, J. Liu and J. Shen,
Chem. Soc. Rev., 2011, 40, 1171; (d) M. Iwaoka, in
Organoselenium Chemistry Between Synthesis and
Biochemistry, ed. C. Santi, Bentham Science Publishers,
Sharjah, 2014, pp. 361–378; (e) S. J. Balkrishna, S. Kumar,
G. K. Azad, B. S. Bhakuni, P. Panini, N. Ahalawat, R. S.
23 M. Iwaoka, T. Takahashi and S. Tomoda, Heteroat. Chem.,
2001, 12, 293.
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