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Catalysis Science & Technology
Page 5 of 6
Journal Name
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ARTICLE
Selected articles, see: (a) A. A. Vieira, J. B. Azeredo, M.
Godoi, C. Santi, E. N. da Silva J. and A. L. Braga, J. Org.
Chem., 2015, 80, 2120; (b) K. K. Casola, D. F. Back and G.
Zeni, J. Org. Chem., 2015, 80, 7702; (c) V. Nascimento, N. L.
Ferreira, R. F. S. Canto, K. L. Schott, E. P. Waczuk, L.
Sancineto, C. Santi, J. B. T. Rocha and A. L. Braga, Eur. J.
DOI: 10.1039/C5CY01395J
4, 49170; (e) L. Yu, J. Wang, X. Zhang, H.-E. Cao, G.-L.
Wang, K.-H. Ding, Q. Xu and M. Lautens, RSC Adv., 2014, 4,
19122; (f) L. Fan, R. Yi, L. Yu, Y.-L. Wu, T. Chen and R.
Guo, Catal. Sci. Technol., 2012, 2, 1136.
Med. Chem., 2014, 87, 131; (d) A. C. Mantovani, T. A. C. 12 Selected articles: (a) M. Jiang, C. Kulsing, Y. Nolvachai and
Goulart, D. F. Back, P. H. Menezes and G. Zeni, J. Org.
Chem., 2014, 79, 10526; (e) B. Hou, D. Benito-Alifonso, R.
Webster, D. Cherns, M. C. Galan and D. J. Fermin, J. Mater.
Chem. A, 2014, 2, 6879; (f) L. Yu, Y.-L. Wu, T. Chen, Y. Pan
and Q. Xu, Org. Lett., 2013, 15, 144.
(a) S. Santoro, J. B. Azeredo, V. Nascimento, L. Sancineto,
A. L. Braga and C. Santi, RSC Adv., 2014, 4, 31521; (b) C.
Santi and C. Tidei, Electrophilic selenium/tellurium reagents:
reactivity and their contribution to Green Chemistry, in: The
Chemistry of Organic Selenium and Tellurium Compounds; Z.
Rappoport, Ed.; John Wiley & Sons, Chichester, 2013; Vol. 4,
pp 569–655.
For reviews, see: (a) D. M. Freudendahl, S. Santoro, S. A.
Shahzad, C. Santi and T. Wirth, Angew. Chem. Int. Ed., 2009, 13 (a) A. Srikrishna, G. Satyanarayana and K. R. Prasad, Synth.
48, 8409; (b) C. Santi, S. Santoro and B. Battistelli, Curr. Org.
Chem., 2010, 14, 2442; (c) A. Breder and S. Ortgies,
Tetrahedron Lett., 2015, 56, 2843; (d) J. Młochowski and H.
Wójtowicz-Młochowska, Molecules, 2015, 20, 10205.
P. J. Marriott, Anal. Chem., 2015, 87, 5753; (b) R. Joshi, A.
Rana and A. Gulati, Food Chem., 2015, 176, 357; (c) M.
Bellotti, A. Salis, A. Grozio, G. Damonte, T. Vigliarolo, A.
Galatini, E. Zocchi, U. Benatti and E. Millo, Bioorg. Med.
Chem., 2015, 23, 22; (d) G. W. Burton, J. Daroszewski, J. G.
Nickerson, J. B. Johnston, T. J. Mogg and G. B. Nikiforov,
Can. J. Chem., 2014, 92, 305; (e) W.-G. Liu, J.-M. Zhou, G.-
Y. Geng, R.-T. Lin and J.-H. Wu, Invest. New Drug., 2014,
32, 227; (f) Q.-S. Shao, Y.-Q. Huang, A.-C. Zhou, H.-P. Guo,
A.-L. Zhang and Y. Wang, J. Sci. Food Agr., 2014, 94, 1430;
(g) T. A. Engler, U. Sampath, S. Naganathan, D. Vander
Velde, F. Takusagawa and D. Yohannes, J. Org. Chem., 1989,
54, 5712.
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Commun., 2007, 37, 1511; (b) A. Srikrishna, L. Shaktikumar
and G. Satyanarayana, ARKIVOC, 2003, 69; (c) A. Bosser, E.
Paplorey and J.-M. Belin, Biotechnol. Prog., 1995, 11, 689;
(d) D. A. Hartman, M. E. Pontones, V. F. Kloss, R. W.
Curley Jr. and L. W. Robertson, J. Nat. Prod., 1988, 51, 947.
The organoselenium compounds are obviously less toxic than
inorganic selenium compounds such as SeO2, H2SeO3 et. al. 14 For detailed conditional optimizations, see ESI.
Moreover, compared with transitional metals, selenium could 15 G. Englert, Helv. Chim. Acta, 1975, 58, 2367.
be metabolized by creatures and is thus much safer to
environment. An adequate englobement of selenium is even
good for health. For details, see: M. P. Rayman, Lancet, 2012,
379, 1256.
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The price in China in August, 2015.
For selected articles, see: (a) L. Sancineto, C. Tidei, L.
Bagnoli, F. Marini, E. J. Lenardao and C. Santi, Molecules,
2015, 20, 10496; (b) C. Santi, R. Di Lorenzo, C. Tidei, L.
Bagnoli and T. Wirth, Tetrahedron, 2012, 68, 10530; (c) S.
Santoro, C. Santi, M. Sabatini, L. Testaferri and M. Tiecco,
Adv. Synth. Catal., 2008, 350, 2881; (d) G.-J. ten Brink, B. C.
M. Fernandes, M. C. A. van Vliet, I. W. C. E. Arends and R.
A. Sheldon, J. Chem. Soc., Perkin Trans. 1, 2001, 224.
(a) L. Yu, H.-Y. Li, X. Zhang, J.-Q. Ye, J.-P. Liu, Q. Xu and
M. Lautens, Org. Lett., 2014, 16, 1346; (b) L. Yu, Y.-L. Wu,
H.-E. Cao, X. Zhang, X.-K. Shi, J. Luan, T. Chen, Y. Pan and
Q. Xu, Green Chem., 2014, 16, 287; (c) X. Zhang, J.-Q. Ye,
L. Yu, X.-K. Shi, M. Zhang, Q. Xu and M. Lautens, Adv.
Synth. Catal., 2015, 357, 955; (d) L. Yu, J. Wang, T. Chen,
Y.-G. Wang and Q. Xu, Appl. Organometal. Chem., 2014, 28,
652; (e) L. Yu, J. Wang, T. Chen, K.-H. Ding and Y. Pan,
Chin. J. Org. Chem., 2013, 33, 1096; (f) L. Yu, J.-Q. Ye, X.
Zhang, Y.-H. Ding and Q. Xu, Catal. Sci. Technol., 2015, 5,
4830.
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A. J. Cresswell, S. T.-C. Eey and S. E. Denmark, Nat. Chem.,
2015, 7, 146.
10 Selected articles: (a) X.-L. Zhang, R.-Z. Guo and X.-D. Zhao,
Org. Chem. Front., 2015, 2, 1334; (b) Z.-M. Deng, J.-L. Wei,
L.-H. Liao, H.-Y. Huang and X.-D. Zhao, Org. Lett., 2015, 17,
1834; (c) F. Chen, C. K. Tan and Y.-Y. Yeung, J. Am. Chem.
Soc., 2013, 135, 1232; (d) J. Trenner, C. Depken, T. Weber
and A. Breder, Angew. Chem. Int. Ed., 2013, 52, 8952; (e) D.
W. Tay, I. T. Tsoi, J. C. Er, G. Y. C. Leung and Y.-Y. Yeung,
Org. Lett., 2013, 15, 1310; (f) F. V. Singh and T. Wirth, Org.
Lett., 2011, 13, 6504.
11 Selected articles: (a) L. Yu, Y.-P. Huang, Z. Wei, Y.-H. Ding,
C.-L. Su and Q. Xu, J. Org. Chem., 2015, 80, 8677; (b) Q. Xu,
H.-M. Xie, P.-L. Chen, L. Yu, J.-H. Chen and X.-G. Hu,
Green Chem., 2015, 17, 2774; (c) L. Xu, J.-J. Huang, Y.-B.
Liu, Y.-N. Wang, B.-L. Xu, K.-H. Ding, Y.-H. Ding, Q. Xu,
This journal is © The Royal Society of Chemistry 20xx
J . Name., 2013, 00, 1-3 | 5
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