Please do not adjust margins
Green Chemistry
Page 6 of 6
COMMUNICATION
Journal Name
7199; e) A. K. Ghosh and M. Brindisi, J. Med. Chem., 2015, 58
,
2895-2940.
details.
DOI: 10.1039/C7GC01449J
5
a) V. Amendola, G. Bergamaschi, M. Boiocchi, L. Fabbrizzi 14 a) At this stage catalytic usage of oximes as a recyclable
and L. Mosca, J. Am. Chem. Soc., 2013, 135, 6345-6355; b) K. template is giving a complex mixture with a trace product.
Kishikawa, S. Nakahara, Y. Nishikawa, S. Kohmoto and M. Currently, we are working on this issue to find the best oxime
Yamamoto, J. Am. Chem. Soc., 2005, 127, 2565-2571; c) Y.-N. functionality and other parameters; b) the recovery of oxime is
Zhao, F. Qureshi, S.-B. Zhang, S.-H. Cui, B. Wang, H.-Y. Chen, H.- only 50%, the probable reason may be due to formation of
T. Lv, S.-F. Zhang and L. Huange, J. Mater. Chem. B., 2014,
2
,
Beckmann product and hydrolysis product acetophenone.
2920-2928.
15 T.-H. Zhu, T.-Q. Wei, S.-Y. Wang and S.-J. Ji, Org. Chem.
6
For selected examples, see: a) K. Lang, J. Park and S. Hong, Front., 2015, 2, 259-264.
Angew. Chem. Int. Ed., 2012, 51, 1620-1624; b) M. Puripat, R.
Ramozzi, M. Hatanaka, W. Parasuk, V. Parasuk and K.
Morokuma, J. Org. Chem., 2015, 80, 6959-6967; c) S. S. So, S.
Oottikkal, J. D. Badjic, C. M. Hadad and A. E. Mattson, J. Org.
Chem., 2014, 79, 4832-4842.
7
a) S. Ozaki, Chem. Rev., 1972, 72, 457-496; b) H. Babad and
A. G. Zeiler, Chem. Rev., 1973, 73, 75-91; c) F. Biggi, R. Maggi and
G. Sartori, Green Chem., 2000, , 140-148.
For selected example on ureas and carbamates synthesis,
2
8
see: a) S. W. Youn and Y. H. Kim, Org. Lett., 2016, 18, 6140-6143;
b) S. H. Kim and S. H. Hong, Org. Lett., 2016, 18, 212-215; c) J.
Zhao, Z. Li, S. Yan, S. Xu, M.-A. Wang, B. Fu and Z. Zhang, Org.
Lett., 2016, 18, 1736-1739; d) M. McLaughlin, M. Palucki and I.
W. Davies, Org. Lett., 2016, 8, 3311-3314; e) W.-H. Rao, X.-S. Yin
and B.-F. Shi, Org. Lett., 2015, 17, 3758-3761; f) J. B. Ernst, N. E.
S. Tay, N. T. Jui and S. L. Buchwald, Org. Lett., 2014, 16, 3844-
3846; g) T.-H. Zhu, X.-P. Xu, J.-J. Cao, T.-Q. Wei, S.-Y. Wang and
S.-J. Jia, Adv. Synth. Catal., 2014, 356, 509-518; h) C. Spyropoulos
and C. G. Kokotos, J. Org. Chem., 2014, 79, 4477-4483; i) K.
Thalluri, S. R. Manne, D. Dev and B. Mandalz, J. Org. Chem.,
2014, 79, 3765-3775; j) E. V. Vinogradova, B. P. Fors and S. L.
Buchwald, J. Am. Chem. Soc., 2012, 134, 11132-11135; k) N. Volz
and J. Clayden, Angew. Chem. Int. Ed., 2011, 50, 12148-2155; l)
H. V. Le and B. Ganem, Org. Lett., 2011, 13, 2584-2585; m) S. L.
Peterson, S. M. Stucka and C. J. Dinsmore, Org. Lett., 2010, 12
,
1340-1343; n) Y. Wei, J. Liu, S. Lin, H. Ding, F. Liang and B. Zhao,
Org. Lett., 2010, 12, 4220-4223; o) S. T. Heller and R. Sarpong,
Org. Lett., 2010, 12, 4572-4575; p) B. J. Kotecki, D. P. Fernando,
A. R. Haight and K. A. Lukin, Org. Lett., 2009, 11, 947-950.
9
For selected examples on carbamates synthesis, see: a) S.
Yoganathan and S. J. Millere, Org. Lett., 2013, 15, 602-605; b) E.
V. Vinogradova, N. H. Park, B. P. Fors and S. L. Buchwald, Org.
Lett., 2013, 15, 1394-1397; c) K. J. Padiya, S. Gavade, B. Kardile,
M. Tiwari, S. Bajare, M. Mane, V. Gaware, S. Varghese, D. Harel
and S. Kurhad, Org. Lett., 2012, 14, 2814-2817; d) P. Dube, N. F.-
F. Nathel, M. Vetelino, M. Couturier, C. L. Aboussafy, S. Pichette,
M. L. Jorgensen and M. Hardink, Org. Lett., 2009, 11, 5622-5625;
e) C. Han and J. A. Porco, Org. Lett., 2007,
Lebel and O. Leogane, Org. Lett., 2006,
Werner and A. G. M. Barrett, J. Org. Chem., 2006, 71, 4302-4304;
h) H. Lebel and O. Leogane, Org. Lett., 2005, , 4107-4110.
9
, 1517-1520; f) H.
8
, 5717-5720; g) T.
7
10 a) G. C. Senadi, B.-C. Guo, W.-P. Hu and J.-J. Wang, Chem.
Commun., 2016, 52, 11410-11413; b) G. C. Senadi, B. S. Gore,
W.-P. Hu and J.-J. Wang, Org. Lett., 2016, 18, 2890-2893; c) S. S.
K. Boominathan and J.-J. Wang, Chem. - Eur. J., 2015, 21, 17044-
17050; d) S. S. K. Boominathan, W.-P. Hu, G. C. Senadi, J. K.
Vandavasi and J.-J. Wang, Chem. Commun., 2014, 51, 6726-6728.
11 a) G. C. Senadi, T.-Y. Lu, G. K. Dhandabani and J.-J. Wang,
Org. Lett., 2017, 19, 1172-1175; b) G. C. Senadi, W.-P. Hu, T.-Y.
Lu, A. M. Garkhedkar, J. K. Vandavasi and J.-J. Wang, Org. Lett.,
2015, 17, 1521-1524; c) G. C. Senadi, W.-P. Hu, S. S. K.
Boominathan and J.-J. Wang, Chem. - Eur. J., 2015, 21, 998-1003.
12 While preparing the manuscript, synthesis of carbamoyl
oximes from isocyanide has been reported by Prof. Jiang and his
co-workers under palladium catalysis, however their purpose is
entirely different, see: W. Hu, J. Li, Y. Xu, J. Li, W. Wu, H. Liu and
H. Jiang, Org. Lett., 2017, 19, 678-681.
6 | J. Name., 2012, 00, 1-3
This journal is © The Royal Society of Chemistry 20xx
Please do not adjust margins