Morpholines. Synthesis and biological activity-Reference-Cited by-同舟云学术

Morpholines. Synthesis and biological activity

Published:2013-06 Issue:6 Volume:49 Page:787-814
ISSN:1070-4280
Container-title:Russian Journal of Organic Chemistry
language:en
Short-container-title:Russ J Org Chem

Author:

Pal’chikov V. A.

Publisher

Pleiades Publishing Ltd

Subject

Organic Chemistry

Link

http://link.springer.com/content/pdf/10.1134/S1070428013060018.pdf

Reference160 articles.

1. Landquist, J.K., Comprehensive Organic Chemistry, Barton, D. and Ollis, W.D., Eds., Oxford: Pergamon, 1979, vol. 4. Kas’yan, L.I., Pal’chikov, V.A., and Tokar’, A.V., Oksazageterotsikly na osnove aminospirtov, epoksidov i aziridinov (Oxaza Heterocycles Based on Amino Alcohols, Epoxides, and Aziridines), Dnepropetrovsk: Dnepropetr. Univ., 2012.

2. Sawargave, S.P., Kudale, A.S., Deore, J.V., Bhosale, D.S., Divse, J.M., Chavan, S.P., and Borate, H.B., Tetrahedron Lett., 2011, vol. 52, p. 5491; Balamurugan, K., Jeyachandran, V., Perumal, S., and Menéndez, J.C., Tetrahedron, 2011, vol. 67, p. 1432; Heravi, M.M., Zakeri, M., and Mohammadi, N., Chin. J. Chem., 2011, vol. 29, p. 1163; Gomes, M.N., De Oliveira, C.M.A., Garrote, C.F.D., De Oliveira, V., and Menegatti, R., Synth. Commun., 2011, vol. 41, p. 52; Heravi, M.M., Zekeri, M., Pooremamy, S., and Oskooie, H.A., Synth. Commun., 2011, vol. 41, p. 113; Song, W., Liu, P., Lei, M., You, H., Chen, X., Chen, H., Ma, L., and Hu, L., Synth. Commun., 2012, vol. 42, p. 236; Guo, M., Zhu, Z., Huang, H., and Zhang, Q., Catal. Commun., 2009, vol. 10, p. 865.

3. Abellan, T., Chinchilla, R., Galindo, N., Najera, C., and Sansano, J.M., J. Heterocycl. Chem., 2000, vol. 37, p. 467.

4. Bera, S. and Panda, G., ACS Comb. Sci., 2012, vol. 14, p. 1.

5. Segat-Dioury, F., Lingibé, O., Graffe, B., Sacquet, M.-C., and Lhommet, G., Tetrahedron, 2000, vol. 56, p. 233.

Cited by 91 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Synthesis, characterization, crystal structure, biological activities, and molecular docking study of the (NHC)Pd(II)(Morp) (NHC: N-heterocyclic carbene, Morp: Morpholine) complexes;Polyhedron;2024-07

2. Exploring the Antiproliferative Potential of Morpholine‐Functionalized Aurones: Design, Synthesis, SAR, DFT, Hirshfeld Surface, 3D Energy Frameworks and Molecular Docking Analysis;ChemistrySelect;2024-05-22

3. Expanding Complex Morpholines Using Systematic Chemical Diversity;Organic Letters;2024-03-20

4. Regioselective synthesis of (Z)‐5‐methylene‐containing morpholin‐2‐ones;Journal of Heterocyclic Chemistry;2024-02-25

5. [4-(2-Aminoethyl)morpholine-κ² N,N′]dibromidocadmium(II): synthesis, crystal structure and Hirshfeld surface analysis;Acta Crystallographica Section E Crystallographic Communications;2024-02-08