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Organic & Biomolecular Chemistry
Page 6 of 8
DOI: 10.1039/C8OB00908B
ARTICLE
Journal Name
Alvaro and H. Garcia, Chem. Commun., 2010, 46, 6476; e)
Y. Dou, X. Huang, H. Wang, L. Yang, H. Li, B. Yuan and G.
Yang, Green Chem., 2017, 19, 2491.
R.-H. Zhu and X.-X. Shi, Synth. Commun., 2012, 42, 1108.
a) M. Szymelfejnik, S. Demkowicz, J. Rachon and D. Witt,
Synthesis, 2007, 2007, 3528; b) S. Antoniow and D. Witt,
Synthesis, 2007, 2007, 363.
Acknowledgements
This work was supported by University of Nevada Las Vegas. Maciej
Kukula at SCAAC is acknowledged for mass spectra data.
7.
8.
Notes and references
9.
a) J. Wang, X. Huang, Z. Ni, S. Wang, Y. Pan and J. Wu,
Tetrahedron, 2015, 71, 7853; b) L. Yang, S. Li, Y. Dou, S.
Zhen, H. Li, P. Zhang, B. Yuan and G. Yang, Asian J. Org.
Chem., 2017, 6, 265; c) F. Hosseinpoor and H.
Golchoubian, Catal. Lett., 2006, 111, 165.
a) N.-S. Li, J. K. Frederiksen and J. A. Piccirilli, Acc. Chem.
Res., 2011, 44, 1257; b) S. Cogoi, V. Rapozzi, F.
Quadrifoglio and L. Xodo, Biochemistry, 2001, 40, 1135; c)
T. S. Kumar, T. Yang, S. Mishra, C. Cronin, S. Chakraborty, J.-
B. Shen, B. T. Liang and K. A. Jacobson, J. Med. Chem.,
2013, 56, 902; d) R. Xie, Q. Zhao, T. Zhang, J. Fang, X. Mei,
J. Ning and Y. Tang, Bioorg. Med. Chem., 2013, 21, 278; e)
B. Kaboudin, S. Emadi and A. Hadizadeh, Bioorg. Chem.,
2009, 37, 101; f) M. Piekutowska and Z. Pakulski,
Carbohydr. Res., 2008, 343, 785.
a) X. Bi, J. Li, F. Meng, H. Wang and J. Xiao, Tetrahedron,
2016, 72, 706; b) J. Bai, X. Cui, H. Wang and Y. Wu, Chem.
Commun., 2014, 50, 8860; c) Y.-C. Liu and C.-F. Lee, Green
Chem., 2014, 16, 357; d) P.-Y. Renard, H. Schwebel, P.
Vayron, L. Josien, A. Valleix and C. Mioskowski, Chem. Eur.
J., 2002, 8, 2910; e) B. Kaboudin, Tetrahedron Lett., 2002,
43, 8713; f) Y.-X. Gao, G. Tang, Y. Cao and Y.-F. Zhao,
Synthesis, 2009, 2009, 1081; g) R. G. Harvey, H. I. Jacobson
and E. V. Jensen, J. Am. Chem. Soc., 1963, 85, 1623; h) G.
Kumaraswamy and R. Raju, Adv. Syn. Catal., 2014, 356,
2591; i) W.-M. Wang, L.-J. Liu, L. Yao, F.-J. Meng, Y.-M. Sun,
C.-Q. Zhao, Q. Xu and L.-B. Han, J. Org. Chem., 2016, 81,
6843; j) S. Kovacs, B. Bayarmagnai, A. Aillerie and L. J.
Goossen, Adv. Syn. Catal., DOI: 10.1002/adsc.201701549,
10.1002/adsc.201701549.
1.
a) L. D. Quin, A guide to organophosphorus chemistry,
Wiley Interscience, New York, 2000; b) K. K. Khoo and R. S.
Norton, in Amino Acids, Peptides and Proteins in Organic
Chemistry, ed. A. B. Hughes, Wiley-VCH Weinheim,
Germany, 2011, 395; c) K. Yamaguchi, K. Sakagami, Y.
Miyamoto, X. Jin and N. Mizuno, Org. Biomol. Chem.,
2014, 12, 9200.
a) T. Tatsuta, M. Hosono, H. Rotinsulu, D. S. Wewengkang,
D. A. Sumilat, M. Namikoshi and H. Yamazaki, J. Nat. Prod.,
2017, 80, 499; b) J. A. Codelli, A. L. A. Puchlopek and S. E.
Reisman, J. Am. Chem. Soc., 2012, 134, 1930; c) M. R.
Vippila, P. K. Ly and G. D. Cuny, J. Nat. Prod., 2015, 78,
2398; d) P. Ramaraju, D. Gergeres, E. Turos, S. Dickey, D. V.
Lim, J. Thomas and B. Anderson, Bioorg. Med. Chem. Lett.,
2012, 22, 3623; e) S. Li, G. Shen and W. Li, Biochemistry,
2018, 57, 258; f) A. Gori, P. Gagni and S. Rinaldi, Chem.
Eur. J., 2017, 23, 14987; g) R. J. Chang and S. Ventura,
Folding of disulfide proteins, Springer, New York, 2011; h)
A. Shaabani, Z. Hezarkhani and E. Badali, RSC Adv., 2015,
5, 61759.
10.
2.
11.
3.
a) J.-G. Wang, Y.-J. Xiao, Y.-H. Li, Y. Ma and Z.-M. Li, Bioorg.
Med. Chem., 2007, 15, 374; b) K.-J. Choi, K. M. Noh, D.-E.
Kim, B. H. Ha, E. E. Kim and M.-Y. Yoon, Arc. Biochem.
Biophys., 2007, 466, 24; c) K.-J. Choi, Y. G. Yu, H. G. Hahn,
J.-D. Choi and M.-Y. Yoon, FEBS Lett., 2005, 579, 4903; d) J.
Shang, W.-M. Wang, Y.-H. Li, H.-B. Song, Z.-M. Li and J.-G.
Wang, J. Agric. Food Chem., 2012, 60, 8286.
4.
5.
A. Vogt, K. Tamura, S. Watson and J. S. Lazo, J. Pharmacol.
Exp. Ther., 2000, 294, 1070.
a) B. Mandal and B. Basu, RSC Adv., 2014, 4, 13854; b) S.
Debasish and B. Babli Roy and Basudeb, Current Med.
Chem., 2017, 24, 4627; c) S. Samanta, S. Ray, A. B. Ghosh
and P. Biswas, RSC Adv., 2016, 6, 39356; d) T. Chatterjee
and B. C. Ranu, RSC Adv., 2013, 3, 10680; e) A.
Christoforou, G. Nicolaou and Y. Elemes, Tetrahedron Lett.,
2006, 47, 9211; f) S. Thurow, V. A. Pereira, D. M. Martinez,
D. Alves, G. Perin, R. G. Jacob and E. J. Lenardão,
Tetrahedron Lett., 2011, 52, 640; g) M. Oba, K. Tanaka, K.
Nishiyama and W. Ando, J. Org. Chem., 2011, 76, 4173; h)
S. Braverman, M. Cherkinsky, Y. Kalendar, R. Jana, M.
Sprecher and I. Goldbergb, Synthesis, 2014, 46, 119; i) S.
Samanta, S. Ray, A. B. Ghosh and P. Biswas, RSC Adv.,
2016, 6, 39356; j) G. Singh, P. K. Khatri, S. K. Ganguly and
S. L. Jain, RSC Adv., 2014, 4, 29124; k) D. H. Scharf, M.
Groll, A. Habel, T. Heinekamp, C. Hertweck, A. A. Brakhage
and E. M. Huber, Angew. Chem., Int. Ed., 2014, 53, 2221; l)
H. T. Abdel-Mohsen, K. Sudheendran, J. Conrad and U.
Beifuss, Green Chem., 2013, 15, 1490; m) A. Corma, T.
Rodenas and M. J. Sabater, Chem. Sci., 2012, 3, 398; n) N.
Iranpoor and B. Zeynizadeh, Synthesis, 1999, 1999, 49.
a) A. Khazaei, M. A. Zolfigol and A. Rostami, Synthesis,
2004, 2004, 2959; b) R. Hunter, M. Caira and N.
Stellenboom, J. Org. Chem., 2006, 71, 8268; c) M. Kirihara,
Y. Asai, S. Ogawa, T. Noguchi, A. Hatano and Y. Hirai,
Synthesis, 2007, 2007, 3286; d) A. Dhakshinamoorthy, M.
12.
a) J. Wang, X. Huang, Z. Ni, S. Wang, J. Wu and Y. Pan,
Green Chem., 2015, 17, 314; b) B. Kaboudin, Y. Abedi, J.-y.
Kato and T. Yokomatsu, Synthesis, 2013, 45, 2323; c) J.-G.
Sun, H. Yang, P. Li and B. Zhang, Org. Lett., 2016, 18, 5114;
d) W. He, X. Hou, X. Li, L. Song, Q. Yu and Z. Wang,
Tetrahedron, 2017, 73, 3133.
Y. Zhu, T. Chen, S. Li, S. Shimada and L.-B. Han, J. Am.
Chem. Soc., 2016, 138, 5825.
S. Song, Y. Zhang, A. Yeerlan, B. Zhu, J. Liu and N. Jiao,
Angew. Chem., Int. Ed., 2017, 56, 2487.
a) T. Hashimoto, D. Hirose and T. Taniguchi, Adv. Syn.
Catal., 2015, 357, 3346; b) A. B. Sorokin, Chem. Rev., 2013,
113, 8152; c) D. Dolphin, T. G. Traylor and L. Y. Xie, Acc.
Chem. Res., 1997, 30, 251; d) M. Costas, Coord. Chem.
Rev., 2011, 255, 2912.
N. Taniguchi, Tetrahedron, 2017, 73, 2030.
A. J. Jasniewski and L. Que, Chemical Rev., 2018, 118,
2554.
13.
14.
15.
16.
17.
18.
19.
20.
21.
J. Stawinski and A. Kraszewski, Acc. Chem. Res., 2002, 35,
952.
M. Abbasi, N. Nowrouzi and S. G. Borazjani, Tetrahedron
Lett., 2017, 58, 4251.
W.-L. Dong, G.-Y. Huang, Z.-M. Li and W.-G. Zhao,
Phosphorus, Sulfur Silicon Relat. Elem., 2009, 184, 2058.
B. P. Bandgar, L. S. Uppalla and V. S. Sadavarte,
6.
6 | J. Name., 2012, 00, 1-3
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