Organic & Biomolecular Chemistry
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DOI: 10.1039/C6OB02413K
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For some recent studies on synthesis of 2-aminobenzothiazoles by
using other methods, see: (a) T. Castanheiro, J. Suffert, M. Gulea
and M. Donnard, Org. Lett., 2016, 18, 2588; (b) J. Zhao, H. Huang,
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amination of benzothiazoles, see: (a) H. Yoon and Y. Lee, J. Org.
Chem., 2015, 80, 10244; (b) S. Mitsuda, T. Fujiwara, K.
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10 For selected references on synthesis of 2-aminobenzothiazoles by
intra-molecular cycliaztion, see: (a) S. Sharma, R. S. Pathare, A. K.
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Purkait, M. A. Ali, R. Paul and T. Punniyamurthy, J. Org. Chem.,
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Bai and Y. Pan, Tetrahedron Lett., 2008, 49, 467; (j) L. L. Joyce, G.
Evindar and R. A. Batey, Chem. Commun., 2004, 446.
40 11 For selected references on synthesis of 2-aminobenzothiazoles by
inter-molecular cycliaztion, see: (a) S. K Sahoo, N. Khatun, A. Gogoi,
A. Deb and B. K. Patel, RSC Adv., 2013, 3, 348; (b) A. Banerjee, S. K.
Santra, S. K. Rout and B. K. Patel, Tetrahedron Lett., 2013, 69, 9096;
(c) R. Yao, H. Liu, Y. Wu and M. Cai, Appl. Organometal. Chem.,
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Adv. Synth. Catal., 2009, 351, 2319; (g) G. Shen, X. Lv and W. Bao,
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Comb. Chem., 2009, 11, 587.
12 For selected references on synthesis of 2-aminobenzothiazoles by
domino condensation/s-arylation/cyclization, see: (a) G. Satish, K.
Harsha Vardhan Reddy, K. Ramesh, K. Karnakar and Y.V.D.
Nageswar, Tetrahedron Lett., 2012, 53, 2518; (b) D. Ma, X. Lu, L.
Shi, H. Zhang, Y. Jiang and X. Liu, Angew. Chem. Int. Ed., 2011, 50,
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13 W. Zeng, P. Dang, X. Zhang, Y. Liang and C. Peng, RSC Adv., 2014, 4,
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60 14 P. Dang, W. Zeng and Y. Liang, Org. Lett., 2015, 17, 34.
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