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I. Zhalolov V. U. Khuzhaev (2004)
10.1023/B:CONC.0000039139.30391.2cChem. Nat. Compd., 40
G. M. Sheldrick (2008)
10.1107/S0108767307043930Acta Crystallogr. A, 64
L. J. Farrugia (2012)
10.1107/S0021889812029111J. Appl. Crystallogr., 45
L. Matesic K. L. Vine (2009)
10.2174/1871520610909040397Anticancer Agents Med. Chem., 9
Y. Guo A. Natarajan (2004)
10.1021/jm0496234J. Med. Chem., 47
B. S. Jensen (2002)
10.1111/j.1527-3458.2002.tb00233.xCNS Drug Rev., 8
M. A. Zolfigol M. Shiri (2010)
10.1021/cr900195aChem. Rev., 110
F. Gallier I. N. Gaisina (2009)
10.1021/jm801317hJ. Med. Chem., 52
Y. P. Sachdeva R. R. Goehring (1985)
10.1021/ja00288a027J. Am. Chem. Soc., 107
L. J. Farrugia (2012)
10.1107/S0021889897003117J. Appl. Crystallogr., 30
S. Aoki M. Kobayashi (1994)
10.1248/cpb.42.2449Chem. Pharm. Bull., 42
K. A. Scheidt C. V. Galliford (2007)
10.1002/anie.200701342Angew Chem. Int. Ed., 46
B. Banerjee G. Brahmachari (2014)
10.1021/sc500575hACS Sustainable Chem. Eng., 2
A. S. Abreu M. R. P. Queiroz (2008)
10.1016/j.bmc.2008.04.004Bioorg. Med. Chem., 16
A. L. Spek (2009)
10.1107/S090744490804362XActa Crystallogr. D, 65
M. S. Chandak S. Selvanayagam (2005)
10.1107/S1600536805027248Acta Crystallogr. E, 61
K. Sethusankar P. Narayanan (2011)
10.1107/S1600536811045491Acta Crystallogr. E, 67
A. P. Dhondge M. G. Kulkarni (2010)
10.3762/bjoc.6.103Beilstein J. Org. Chem., 6
I. Oka R. Veluri (2003)
10.1021/np030288gJ. Nat. Prod., 66
S. J. Danishefsky H. Lin (2003)
10.1002/anie.200390048Angew Chem. Int. Ed., 42
S. Carmeli R. Bell (1994)
10.1021/np50113a022J. Nat. Prod., 57
H. P. Zhang Y. Kamano (1995)
10.1016/0040-4039(95)00395-STetrahedron Lett., 36
D. Yean W. R. Chao (2007)
10.1021/jm070040eJ. Med. Chem., 50
S. Saito T. Kagata (2006)
10.1021/np0602968J. Nat. Prod., 69
S. Burnelli A. andreani (2008)
10.1021/jm800194kJ. Med. Chem., 51
M. Marzi G. Giannini (2009)
10.1016/j.bmcl.2009.03.101Bioorg. Med. Chem. Lett., 19
J. K. MacLeod H. B. Rasmussen (1997)
10.1021/np970246qJ. Nat. Prod., 60
M. Nardelli (1995)
10.1107/S0021889895007138J. Appl. Crystallogr., 28
I. Sattler Y. Q. Tang (2001)
10.1002/1099-0690(200101)2001:2<261::AID-EJOC261>3.0.CO;2-6Eur. J. Org. Chem., 66
Abstract The new biologically relevant compound, 5,5″-methoxy-1′-methyl-1H,1″H-[3,3′:3′,3″-terindol]-2′(1′H)-one was synthesized, in 89% yield, by the one-pot reaction between 5-methoxyindole and 1-methylisatin in the presence of a low-cost and environmentally benign commercially available sulfamic acid as an organocatalyst and have been characterized by elemental analyses, IR spectra, and single crystal X-ray analysis. The crystals are orthorhombic, sp. gr. Pbca, Z = 8. The structure is stabilized by N–H···O and C–H···O interactions.
Crystallography Reports – Springer Journals
Published: Nov 1, 2017
Keywords: Crystallography and Scattering Methods
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