2015
DOI: 10.1002/chin.201512105
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ChemInform Abstract: Mild, Stereoselective, and Highly Efficient Synthesis of N‐Acylhydrazones Mediated by CeCl3·7H2O in a Broad Range of Solvents.

Abstract: The catalyst is active in various protic and aprotic solvents including water, but EtOH is the medium of choice.

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“…The analysis of the 1 H NMR spectra revealed that compounds 15a−15h exist as Z/E isomers, and the proportion of isomers can be determined according to the literature methods. 28,29 Phytotoxic Activity. The phytotoxic-activity tests (according to the criterion of safety evaluation of pesticide to crops: NYT 1965.1-2010) revealed that compounds 3a−3c, 4, 5, 8, 10, 11, 12a−12d, 13a−13l, 14, and 15a−15h were safe for testing on plants at 500 μg/mL.…”
Section: ■ Results and Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…The analysis of the 1 H NMR spectra revealed that compounds 15a−15h exist as Z/E isomers, and the proportion of isomers can be determined according to the literature methods. 28,29 Phytotoxic Activity. The phytotoxic-activity tests (according to the criterion of safety evaluation of pesticide to crops: NYT 1965.1-2010) revealed that compounds 3a−3c, 4, 5, 8, 10, 11, 12a−12d, 13a−13l, 14, and 15a−15h were safe for testing on plants at 500 μg/mL.…”
Section: ■ Results and Discussionmentioning
confidence: 99%
“…1 H NMR (400 MHz, CDCl 3 ): δ 8.00 (s, 2H, indole-NH), 7.64 (d, J = 8.0 Hz, 2H, Ar−H), 7.36 (t, J = 8.4 Hz, 4H, Ar−H), 7 29. (d, J = 7.0 Hz, 1H, Ar−H), 7.18−7.24 (m, 3H, Ar−H), 6.99−7.08 (m, 5H, Ar−H), 6.63 (d, J = 7.8 Hz, 1H, CH 2 −NH), 6.17 (s, 1H, CH 2 NHCS−NH), 4.97 (t, J = 7.1 Hz, 1H, Ar 2 −CH), 4.43 (t, J = 5.4 Hz, 2H, CH 2 ); 13 C NMR (100 MHz, DMSO-d 6 ): δ 180.4, 139.6, 137.0, 130.4, 129.0, 127.2, 124.4, 123.2, 123.0, 121.4, 119.5, 118.7, 116.5, 111.9, 48.9, 33.5.…”
mentioning
confidence: 99%